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Article

Screen for usher syndrome 1B mutations in the ovine myosin VIIa gene.

Advances in experimental medicine and biology - 1 Jan 2003

Slatter Tania, Azarian Sassan M, Tebbutt Scott, Maw Marion, Williams David S

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Identifiers

PMID: 15180259
DOI: 10.1007/978-1-4615-0067-4_19

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Related research

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Screen for usher syndrome 1B mutations in the ovine myosin VIIa gene.PMID 15180259Read ↗

Identification of a new mutation of the myosin VII head region in Usher syndrome type 1.Semantic proximity Read ↗

Mutations in the myosin VIIA gene cause a wide phenotypic spectrum, including atypical Usher syndrome.Semantic proximity Read ↗

MYO7A mutation screening in Usher syndrome type I patients from diverse origins.Semantic proximity Read ↗

Mutation profile of all 49 exons of the human myosin VIIA gene, and haplotype analysis, in Usher 1B families from diverse origins.Semantic proximity Read ↗

Twelve novel myosin VIIA mutations in 34 patients with Usher syndrome type I: confirmation of genetic heterogeneity.Semantic proximity Read ↗

Two Finnish USH1B patients with three novel mutations in myosin VIIA.Semantic proximity Read ↗

Molecular cloning and domain structure of human myosin-VIIa, the gene product defective in Usher syndrome 1B.Semantic proximity Read ↗

Analysis of MYO7A in a Moroccan family with Usher syndrome type 1B: novel loss-of-function mutation and non-pathogenicity of p.Y1719C.Semantic proximity Read ↗

Defective myosin VIIA gene responsible for Usher syndrome type 1B.Semantic proximity Read ↗

Five novel KIT mutations in horses with white coat colour phenotypes.Semantic proximity Read ↗

Identification of three novel mutations in the MYO7A gene.Semantic proximity Read ↗

Myosin VIIA mutation screening in 189 Usher syndrome type 1 patients.Semantic proximity Read ↗

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