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Article

Identification and functional analysis of a novel mutation in the SOX10 gene associated with Waardenburg syndrome type IV

16 Jan 2014

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 24440785
DOI: 10.1016/j.gene.2014.01.026

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Related research

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Research trail→

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Identification and functional analysis of a novel mutation in the SOX10 gene associated with Waardenburg syndrome type IVPMID 24440785Read ↗

SOX10 mutations in patients with Waardenburg-Hirschsprung diseaseSemantic proximity Read ↗

Alu-mediated deletion of SOX10 regulatory elements in Waardenburg syndrome type 4Semantic proximity Read ↗

A De Novo Mutation in SOX10 in a Chinese Boy with Waardenburg Syndrome Type 2.Semantic proximity Read ↗

A de novo deletion mutation in SOX10 in a Chinese family with Waardenburg syndrome type 4.Semantic proximity Read ↗

Waardenburg syndrome type IIE in a Japanese patient caused by a novel non-frame-shift duplication mutation in the SOX10 gene.Semantic proximity Read ↗

Novel mutations in the SOX10 gene in the first two Chinese cases of type IV Waardenburg syndrome.Semantic proximity Read ↗

A Novel Mutation of the SOX10 Gene Associated with Waardenburg Syndrome Type IVSemantic proximity Read ↗

Identification and functional analysis of SOX10 missense mutations in different subtypes of Waardenburg syndrome.Semantic proximity Read ↗

A de novo SOX10 mutation causing severe type 4 Waardenburg syndrome without Hirschsprung disease.Semantic proximity Read ↗

A novel variant of the SOX10 gene associated with Waardenburg syndrome type IV.Semantic proximity Read ↗

A de novo mutation of the SOX10 gene associated with inner ear malformation in a Guangxi family with Waardenburg syndrome type II.Semantic proximity Read ↗

Functional analysis of a SOX10 gene mutation associated with Waardenburg syndrome II.Semantic proximity Read ↗

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