(Q28253373)

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Autosomal dominant non-syndromic deafness caused by a mutation in the myosin VIIA gene

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Autosomal dominant non-syndromic deafness caused by a mutation in the myosin VIIA gene (English)

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1 reference

X Z Liu

1

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J Walsh

series ordinal

2

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Y Tamagawa

series ordinal

3

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K Kitamura

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4

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M Nishizawa

series ordinal

5

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K P Steel

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6

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S D Brown

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7

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language of work or name

English

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publication date

November 1997

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published in

Nature Genetics

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volume

17

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issue

3

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page(s)

268-9

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cites work

Connexin 26 mutations in hereditary non-syndromic sensorineural deafness

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Crossref

reference URL

https://api.crossref.org/works/10.1038/NG1197-268

retrieved

21 April 2017

A gene for a dominant form of non-syndromic sensorineural deafness (DFNA11) maps within the region containing the DFNB2 recessive deafness gene

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038/NG1197-268

retrieved

21 April 2017

Defective myosin VIIA gene responsible for Usher syndrome type 1B

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038/NG1197-268

retrieved

21 April 2017

Mutations in the myosin VIIA gene cause non-syndromic recessive deafness

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038/NG1197-268

retrieved

21 April 2017

The autosomal recessive isolated deafness, DFNB2, and the Usher 1B syndrome are allelic defects of the myosin-VIIA gene

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038/NG1197-268

retrieved

21 April 2017

Myosin VIIA gene: heterogeneity of the mutations responsible for Usher syndrome type IB

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038/NG1197-268

retrieved

21 April 2017

Human myosin VIIA responsible for the Usher 1B syndrome: a predicted membrane-associated motor protein expressed in developing sensory epithelia

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038/NG1197-268

21 April 2017

1 reference

https://api.crossref.org/works/10.1038%2FNG1197-268

retrieved

21 January 2018

A human gene responsible for neurosensory, non-syndromic recessive deafness is a candidate homologue of the mouse sh-1 gene

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stated in

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reference URL

https://api.crossref.org/works/10.1038%2FNG1197-268

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7 January 2021

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Identifiers

DOI

10.1038/NG1197-268

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PubMed publication ID

9354784

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(Q28253373)

Autosomal dominant non-syndromic deafness caused by a mutation in the myosin VIIA gene

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