Frequency of mtDNA A1555G and A7445G mutations among children with prelingual deafness in Turkey (Q48355437)

10 February 2018

title

Frequency of mtDNA A1555G and A7445G mutations among children with prelingual deafness in Turkey (English)

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M Tekin

1

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T Duman

2

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G Boğoçlu

3

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A İncesulu

4

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E Çomak

5

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S Fitoz

6

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E Yılmaz

7

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I İlhan

8

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N Akar

9

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publication date

21 January 2003

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European Journal of Pediatrics

published in

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volume

162

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issue

3

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page(s)

154-158

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Three novel connexin26 gene mutations in autosomal recessive non-syndromic deafness

cites work

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12 December 2020

Prevalent connexin 26 gene (GJB2) mutations in Japanese

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12 December 2020

Heterogenous point mutations in the mitochondrial tRNA Ser(UCN) precursor coexisting with the A1555G mutation in deaf students from Mongolia

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12 December 2020

Maternally inherited cardiomyopathy: an atypical presentation of the mtDNA 12S rRNA gene A1555G mutation

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12 December 2020

Maternally inherited hearing impairment

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12 December 2020

Prevalence of mitochondrial gene mutations among hearing impaired patients

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12 December 2020

Novel mutations in the connexin 26 gene (GJB2) responsible for childhood deafness in the Japanese population

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12 December 2020

Connexin26 mutations associated with nonsyndromic hearing loss

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12 December 2020

Familial progressive sensorineural deafness is mainly due to the mtDNA A1555G mutation and is enhanced by treatment of aminoglycosides

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12 December 2020

A novel mitochondrial point mutation in a maternal pedigree with sensorineural deafness.

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12 December 2020

The A1555G mutation in the 12S rRNA gene of human mtDNA: recurrent origins and founder events in families affected by sensorineural deafness

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12 December 2020

Inherited susceptibility to aminoglycoside ototoxicity: genetic heterogeneity and clinical implications

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12 December 2020

Mitochondrial A7445G mutation in two pedigrees with palmoplantar keratoderma and deafness

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12 December 2020

A biochemical basis for the inherited susceptibility to aminoglycoside ototoxicity

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12 December 2020

Advances in hereditary deafness

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Mutation in the mitochondrial 12S rRNA gene in two families from Mongolia with matrilineal aminoglycoside ototoxicity

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12 December 2020

Mitochondrial ribosomal RNA gene mutation in a patient with sporadic aminoglycoside ototoxicity

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12 December 2020

Connexin 26 gene (GJB2) mutation modulates the severity of hearing loss associated with the 1555A-->G mitochondrial mutation

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12 December 2020

Connexin 26 (GJB2) mutations in the Turkish population: implications for the origin and high frequency of the 35delG mutation in Caucasians

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12 December 2020

Prevalence of mitochondrial DNA mutations in childhood/congenital onset non-syndromal sensorineural hearing impairment

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12 December 2020

Mitochondrial ribosomal RNA mutation associated with both antibiotic–induced and non–syndromic deafness

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12 December 2020

Mitochondrial mutation associated with nonsyndromic deafness

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12 December 2020

Coexistence of factor V 1691 G-A and factor V 4070 A-G mutation in turkish thromboembolic patients

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12 December 2020

10.1007/S00431-002-1129-Z

Identifiers

DOI

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10 February 2018

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10 February 2018