Biallelic Mutation of BEST1 Causes a Distinct Retinopathy in Humans-Reference-Cited by-同舟云学术

Biallelic Mutation of BEST1 Causes a Distinct Retinopathy in Humans

Published:2008-01 Issue:1 Volume:82 Page:19-31
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Burgess Rosemary,Millar Ian D.,Leroy Bart P.,Urquhart Jill E.,Fearon Ian M.,De Baere Elfrida,Brown Peter D.,Robson Anthony G.,Wright Genevieve A.,Kestelyn Philippe,Holder Graham E.,Webster Andrew R.,Manson Forbes D.C.,Black Graeme C.M.

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference29 articles.

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4. The vitelliform macular dystrophy protein defines a new family of chloride channels;Sun;Proc. Natl. Acad. Sci. USA,2002

5. Structure-function analysis of the bestrophin family of anion channels;Tsunenari;J. Biol. Chem.,2003

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