c.G2114A MYH9 mutation (DFNA17) causes non-syndromic autosomal dominant hearing loss in a Brazilian family.

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Genetic Linkage Analysis of DFNB3, DFNB9 and DFNB21 Loci in GJB2 Negative Families with Autosomal Recessive Non-syndromic Hearing Loss.Targeted Resequencing of Deafness Genes Reveals a Founder MYO15A Variant in Northeastern Brazil.

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c.G2114A MYH9 mutation (DFNA17) causes non-syndromic autosomal dominant hearing loss in a Brazilian family.

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c.G2114A MYH9 mutation (DFNA17 ...... ng loss in a Brazilian family.

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c.G2114A MYH9 mutation (DFNA17 ...... ng loss in a Brazilian family.

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c.G2114A MYH9 mutation (DFNA17 ...... ng loss in a Brazilian family.

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c.G2114A MYH9 mutation (DFNA17 ...... ing loss in a Brazilian family

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Carolina Fischinger Moura de Souza

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Guilherme L Yamamoto

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Simone Gomes Ferreira

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Vitor G L Dantas

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P2860

Human nonsyndromic hereditary deafness DFNA17 is due to a mutation in nonmuscle myosin MYH9

A novel locus (DFNA23) for prelingual autosomal dominant nonsyndromic hearing loss maps to 14q21-q22 in a Swiss German kindred

Nonsyndromic hearing impairment: unparalleled heterogeneity

Merlin--rapid analysis of dense genetic maps using sparse gene flow trees

A method and server for predicting damaging missense mutations

Mutations in a novel cochlear gene cause DFNA9, a human nonsyndromic deafness with vestibular dysfunction

A gene for non-syndromic autosomal dominant progressive postlingual sensorineural hearing loss maps to chromosome 14q12-13

ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data

Fast and accurate long-read alignment with Burrows-Wheeler transform

Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm

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616-621

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scholarly article

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10.1590/S1415-47572014005000025

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Karina Lezirovitz

Regina Celia Mingroni Netto

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2014-10-01T00:00:00Z

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25505834

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c.G2114A MYH9 mutation (DFNA17) causes non-syndromic autosomal dominant hearing loss in a Brazilian family.

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P2860

P2860

c.G2114A MYH9 mutation (DFNA17) causes non-syndromic autosomal dominant hearing loss in a Brazilian family.

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