(Q48355437)

10 February 2018

title

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

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10 February 2018

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M Tekin

1

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10 February 2018

T Duman

2

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10 February 2018

G Boğoçlu

3

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10 February 2018

A İncesulu

4

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E Çomak

5

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S Fitoz

6

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10 February 2018

E Yılmaz

7

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I İlhan

8

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N Akar

9

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10 February 2018

publication date

21 January 2003

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10 February 2018

European Journal of Pediatrics

published in

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10 February 2018

volume

162

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10 February 2018

issue

3

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10 February 2018

page(s)

154-158

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10 February 2018

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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12 December 2020

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