Heterogeneity of Hereditary Hearing Loss in Iran: a Comprehensive Review. - Wikidata - awgldk - TriplyDB

Heterogeneity of Hereditary Hearing Loss in Iran: a Comprehensive Review.

Heterogeneity of Hereditary Hearing Loss in Iran: a Comprehensive Review.

http://www.wikidata.org/entity/Q30244548

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The conserved p.Arg108 residue in S1PR2 (DFNB68) is fundamental for proper hearing: evidence from a consanguineous Iranian family.

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Heterogeneity of Hereditary Hearing Loss in Iran: a Comprehensive Review.

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description

2016 nî lūn-bûn

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2016 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2016 թվականի հոտեմբերին հրատարակված գիտական հոդված

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2016年の論文

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2016年論文

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2016年論文

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2016年論文

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2016年論文

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2016年論文

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2016年论文

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name

Heterogeneity of Hereditary Hearing Loss in Iran: a Comprehensive Review.

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Heterogeneity of Hereditary Hearing Loss in Iran: a Comprehensive Review.

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type

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Heterogeneity of Hereditary Hearing Loss in Iran: a Comprehensive Review.

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Heterogeneity of Hereditary Hearing Loss in Iran: a Comprehensive Review.

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Heterogeneity of Hereditary Hearing Loss in Iran: a Comprehensive Review.

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Heterogeneity of Hereditary Hearing Loss in Iran: a Comprehensive Review.

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Archives of Iranian Medicine

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Heterogeneity of Hereditary Hearing Loss in Iran: a Comprehensive Review.

@en

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Ahmad Daneshi

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Christina Sloan-Heggen

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Diana Kolbe

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Hela Azaiez

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Hossein Najmabadi

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Kathy Frees

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Kevin Booth

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Kimia Kahrizi

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Maryam Beheshtian

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Marzieh Mohseni

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P2860

Mutation of COL11A2 causes autosomal recessive non-syndromic hearing loss at the DFNB53 locus

Pendred syndrome is caused by mutations in a putative sulphate transporter gene (PDS)

Waardenburg syndrome

SLC26A4 genotypes and phenotypes associated with enlargement of the vestibular aqueduct

Brown-Vialetto-Van Laere syndrome and Fazio-Londe disease - treatable motor neuron diseases of childhood

Characterising the spectrum of autosomal recessive hereditary hearing loss in Iran

PDZD7 and hearing loss: More than just a modifier

A deletion involving the connexin 30 gene in nonsyndromic hearing impairment

Gap junctions in the rat cochlea: immunohistochemical and ultrastructural analysis

Contribution of connexin26 (GJB2) mutations and founder effect to non-syndromic hearing loss in India

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720-728

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0161910/AIM.0010

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