A Common Ancestral Origin of the Frequent and Widespread 2299delG USH2A Mutation-Reference-Cited by-同舟云学术

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A Common Ancestral Origin of the Frequent and Widespread 2299delG USH2A Mutation

Published:2001-07 Issue:1 Volume:69 Page:228-234
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Dreyer Bo,Tranebjærg Lisbeth,Brox Vigdis,Rosenberg Thomas,Möller Claes,Beneyto Magdalena,Weston Michael D.,Kimberling William J.,Nilssen Øivind

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference11 articles.

1. Three novel mutations and twelve polymorphisms identified in the USH2A gene in Israeli USH2 families;Adato;Hum Mutat,2000

2. Prevalence of 2314delG mutation in Spanish patients with Usher syndrome type II (USH2);Beneyto;Ophthalmic Genet,2000

3. Usher syndrome: definition and estimate of prevalence from two high-risk populations;Boughman;J Chronic Dis,1983

4. Identification of novel USH2A mutations: implications for the structure of USH2A protein;Dreyer;Eur J Hum Genet,2000

5. Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa;Eudy;Science,1998

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