(Q50485978)

14 March 2018

title

Identification of 605ins46, a novel GJB2 mutation in a Japanese family. (English)

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14 March 2018

author name string

Isamu Yuge

1

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14 March 2018

Akihiro Ohtsuka

2

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14 March 2018

Tatsuo Matsunaga

3

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14 March 2018

Shin-ichi Usami

4

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14 March 2018

publication date

1 October 2002

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14 March 2018

number of pages

4

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inferred from page(s)

published in

Auris Nasus Larynx

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14 March 2018

volume

29

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14 March 2018

issue

4

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14 March 2018

page(s)

379-382

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14 March 2018

Genetic epidemiology of hearing impairment

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0385-8146%2802%2900055-X

7 January 2021

Genetic epidemiological studies of early-onset deafness in the U.S. school-age population

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https://api.crossref.org/works/10.1016%2FS0385-8146%2802%2900055-X

7 January 2021

Connexin 26 mutations in hereditary non-syndromic sensorineural deafness

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https://api.crossref.org/works/10.1016%2FS0385-8146%2802%2900055-X

7 January 2021

Prelingual deafness: high prevalence of a 30delG mutation in the connexin 26 gene

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https://api.crossref.org/works/10.1016%2FS0385-8146%2802%2900055-X

7 January 2021

Connexin-26 mutations in sporadic and inherited sensorineural deafness

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https://api.crossref.org/works/10.1016%2FS0385-8146%2802%2900055-X

7 January 2021

Novel mutations in the connexin 26 gene (GJB2) that cause autosomal recessive (DFNB1) hearing loss

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https://api.crossref.org/works/10.1016%2FS0385-8146%2802%2900055-X

7 January 2021

Prevalent connexin 26 gene (GJB2) mutations in Japanese

1 reference

https://api.crossref.org/works/10.1016%2FS0385-8146%2802%2900055-X

7 January 2021

Connexin26 mutations associated with the most common form of non-syndromic neurosensory autosomal recessive deafness (DFNB1) in Mediterraneans

1 reference

https://api.crossref.org/works/10.1016%2FS0385-8146%2802%2900055-X

7 January 2021

Molecular basis of childhood deafness resulting from mutations in the GJB2 (connexin 26) gene.

1 reference

https://api.crossref.org/works/10.1016%2FS0385-8146%2802%2900055-X

7 January 2021

A Moroccan family with autosomal recessive sensorineural hearing loss caused by a mutation in the gap junction protein gene connexin 26 (GJB2).

1 reference

https://api.crossref.org/works/10.1016%2FS0385-8146%2802%2900055-X

7 January 2021

Connexin26 mutations associated with nonsyndromic hearing loss.

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https://api.crossref.org/works/10.1016%2FS0385-8146%2802%2900055-X

7 January 2021

Mutations in the connexin 26 gene (GJB2) among Ashkenazi Jews with nonsyndromic recessive deafness

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https://api.crossref.org/works/10.1016%2FS0385-8146%2802%2900055-X

7 January 2021

A common founder for the 35delG GJB2 gene mutation in connexin 26 hearing impairment.

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7 January 2021

Detection of sequence variability of the collagen type IIalpha 1 3' variable number of tandem repeat

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https://api.crossref.org/works/10.1016%2FS0385-8146%2802%2900055-X

7 January 2021

Clinical features of the prevalent form of childhood deafness, DFNB1, due to a connexin-26 gene defect: implications for genetic counselling.

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https://api.crossref.org/works/10.1016%2FS0385-8146%2802%2900055-X

7 January 2021

Identification of the protein product of the Coch gene (hereditary deafness gene) as the major component of bovine inner ear protein.

1 reference

https://api.crossref.org/works/10.1016%2FS0385-8146%2802%2900055-X

7 January 2021

10.1016/S0385-8146(02)00055-X

Identifiers

DOI

1 reference

14 March 2018

1 reference

14 March 2018