Twelve novel myosin VIIA mutations in 34 patients with Usher syndrome type I: Confirmation of genetic heterogeneity-Reference-Cited by-同舟云学术

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Twelve novel myosin VIIA mutations in 34 patients with Usher syndrome type I: Confirmation of genetic heterogeneity

Published:1999 Issue:2 Volume:13 Page:133-140
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Janecke Andreas R.,Meins Moritz,Sadeghi Mojy,Grundmann Kathrin,Apfelstedt-Sylla Eckart,Zrenner Eberhart,Rosenberg Thomas,Gal Andreas

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference22 articles.

1. Mutation Profile of All 49 Exons of the Human Myosin VIIA Gene, and Haplotype Analysis, in Usher 1B Families from Diverse Origins

2. 1996. Simple and nonisotopic methods to detect unknown gene mutations in nucleic acids. In: editor. Methods in molecular genetics. Vol 8. Orlando, FLAcademic Press. p 26-39

3. Molecular Cloning and Domain Structure of Human Myosin-VIIa, the Gene Product Defective in Usher Syndrome 1B

4. Phylogenetic analysis of the myosin superfamily

5. Conservation within the myosin motor domain: implications for structure and function

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