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Article

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

American journal of human genetics - 1 Sept 1998

Liu X Z, Hope C, Walsh J, Newton V, Ke X M, Liang C Y, Xu L R, Zhou J M, Trump D, Steel K P, Bundey S, Brown S D

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 9718356
DOI: 10.1086/302026
PMCID: PMC1377414

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Related research

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Click a neighbor to travelStep 1 · 12 closest

Mutations in the myosin VIIA gene cause a wide phenotypic spectrum, including atypical Usher syndrome.PMID 9718356Read ↗

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

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

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

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

The usher syndromes.Semantic proximity Read ↗

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

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

Mutations in myosin VIIA (MYO7A) and usherin (USH2A) in Spanish patients with Usher syndrome types I and II, respectively.Semantic proximity Read ↗

Extended mutation spectrum of Usher syndrome in Finland.Semantic proximity Read ↗

[Genetics of Usher syndrome].Semantic proximity Read ↗

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