Characterising the spectrum of autosomal recessive hereditary hearing loss in Iran (Q27317126)

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26 February 2020

title

Characterising the spectrum of autosomal recessive hereditary hearing loss in Iran (English)

1 reference

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1 reference

1 reference

28

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26 February 2020

Hasan Otukesh

18

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26 February 2020

Ahmad Daneshi

23

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26 February 2020

Mohammad Farhadi

24

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Kimia Kahrizi

25

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26 February 2020

Richard J Smith

26

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26 February 2020

author name string

Christina M Sloan-Heggen

1

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26 February 2020

Mojgan Babanejad

2

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26 February 2020

Maryam Beheshtian

3

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26 February 2020

Allen C Simpson

4

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26 February 2020

Kevin T Booth

5

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26 February 2020

Fariba Ardalani

6

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26 February 2020

Kathy L Frees

7

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26 February 2020

Marzieh Mohseni

8

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26 February 2020

Reza Mozafari

9

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26 February 2020

Zohreh Mehrjoo

10

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26 February 2020

Leila Jamali

11

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26 February 2020

Saeideh Vaziri

12

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26 February 2020

Tara Akhtarkhavari

13

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26 February 2020

Niloofar Bazazzadegan

14

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26 February 2020

Nooshin Nikzat

15

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26 February 2020

Sanaz Arzhangi

16

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26 February 2020

Farahnaz Sabbagh

17

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26 February 2020

Seyed Morteza Seifati

19

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26 February 2020

Hossein Khodaei

20

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26 February 2020

Maryam Taghdiri

21

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26 February 2020

Nicole C Meyer

22

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26 February 2020

Hela Azaiez

27

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26 February 2020

language of work or name

English

0 references

publication date

7 October 2015

1 reference

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Journal of Medical Genetics

26 February 2020

published in

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26 February 2020

volume

52

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26 February 2020

issue

12

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26 February 2020

page(s)

823-829

1 reference

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PDZD7 and hearing loss: More than just a modifier

26 February 2020

cites work

1 reference

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21 March 2017

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Mutations in LOXHD1, an evolutionarily conserved stereociliary protein, disrupt hair cell function in mice and cause progressive hearing loss in humans

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Mutation of COL11A2 causes autosomal recessive non-syndromic hearing loss at the DFNB53 locus

21 March 2017

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Genetic analysis through OtoSeq of Pakistani families segregating prelingual hearing loss

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Targeted genomic capture and massively parallel sequencing to identify genes for hereditary hearing loss in Middle Eastern families

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Loss-of-function mutations of ILDR1 cause autosomal-recessive hearing impairment DFNB42

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28 September 2017

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Two missense mutations in SLC26A4 gene: a molecular and functional study

28 September 2017

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Five novel loci for inherited hearing loss mapped by SNP-based homozygosity profiles in Palestinian families

28 September 2017

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28 September 2017

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21 January 2018

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Molecular analysis of SLC26A4 gene in patients with nonsyndromic hearing loss and EVA: identification of two novel mutations in Brazilian patients

21 January 2018

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Analysis of the thyroid phenotype in 42 patients with Pendred syndrome and nonsyndromic enlargement of the vestibular aqueduct

21 January 2018

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Genome-wide SNP genotyping identifies the Stereocilin (STRC) gene as a major contributor to pediatric bilateral sensorineural hearing impairment

21 January 2018

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GJB2 mutations: passage through Iran

21 January 2018

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PubMed

https://pubmed.ncbi.nlm.nih.gov/26445815

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

A comprehensive study to determine heterogeneity of autosomal recessive nonsyndromic hearing loss in Iran

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/26445815

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1136/JMEDGENET-2015-103389

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26445815 AND SRC:MED&resulttype=core&format=json

26 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26445815 AND SRC:MED&resulttype=core&format=json

26 February 2020

PubMed publication ID

26445815

1 reference