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Article

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

Human mutation - 1 Jan 1997

Liu X Z, Newton V E, Steel K P, Brown S D

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Identifiers

PMID: 9259201
DOI: 10.1002/(SICI)1098-1004(1997)10:2<168::AID-HUMU10>3.0.CO;2-Y

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Related research

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Click a neighbor to travelStep 1 · 12 closest

Identification of a new mutation of the myosin VII head region in Usher syndrome type 1.PMID 9259201Read ↗

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

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

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

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

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

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

Identification of three novel mutations in the USH1C gene and detection of thirty-one polymorphisms used for haplotype analysis.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 ↗

New splice site mutations in MYO7A causing Usher syndrome type 1: a study on a Chinese consanguineous family.Semantic proximity Read ↗

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

Characterization of Usher syndrome type I gene mutations in an Usher syndrome patient population.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 ↗

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