Genetic Linkage Analysis of 15 DFNB Loci in a Group of Iranian Families with Autosomal Recessive Hearing Loss. (Q36349189)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23113071 AND SRC:MED&resulttype=core&format=json

16 February 2020

title

Genetic Linkage Analysis of 15 DFNB Loci in a Group of Iranian Families with Autosomal Recessive Hearing Loss (English)

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16 February 2020

1 reference

Ma Tabatabaiefar

1

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16 February 2020

F Alasti

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16 February 2020

M Montazer Zohour

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16 February 2020

L Shariati

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16 February 2020

E Farrokhi

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16 February 2020

Dd Farhud

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16 February 2020

Gv Camp

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16 February 2020

Mr Noori-Daloii

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16 February 2020

M Hashemzadeh Chaleshtori

9

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16 February 2020

language of work or name

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30 June 2011

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Iranian Journal of Public Health

16 February 2020

published in

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16 February 2020

volume

40

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16 February 2020

issue

2

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16 February 2020

page(s)

34-48

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Variable hearing impairment in a DFNB2 family with a novel MYO7A missense mutation

16 February 2020

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30 September 2017

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22 September 2018

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Identifiers

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16 February 2020

PubMed publication ID

23113071

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