Mutations in the Myosin VIIA Gene Cause a Wide Phenotypic Spectrum, Including Atypical Usher Syndrome-Reference-Cited by-同舟云学术

Mutations in the Myosin VIIA Gene Cause a Wide Phenotypic Spectrum, Including Atypical Usher Syndrome

Published:1998-09 Issue:3 Volume:63 Page:909-912
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Liu Xue-Zhong,Hope Carolyn,Walsh James,Newton Valerie,Ke Xiao Mei,Liang Chuan Yu,Xu Li Ron,Zhou Jiu Mu,Trump Dorothy,Steel Karen P.,Bundey Sarah,Brown Steve D.M.

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference16 articles.

1. Mutation profile of all 49 exons of the human myosin VIIA gene, and haplotype analysis, in Usher 1B families from diverse origins;Adato;Am J Hum Genet,1997

2. Molecular cloning and domain structure of human myosin VIIa, the gene product defective in Usher syndrome 1B;Chen;Genomics,1996

3. Conservation within the myosin motor domain: implications for structure and function;Cope;Structure,1996

4. Unconventional myosins, the basis for deafness in mouse and man;Hasson;Am J Hum Genet,1997

5. Usher syndrome in the city of Birmingham—prevalence and clinical classification;Hope;Br J Ophthalmol,1997

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