A Mutation in SLC24A1 Implicated in Autosomal-Recessive Congenital Stationary Night Blindness-Reference-Cited by-同舟云学术

A Mutation in SLC24A1 Implicated in Autosomal-Recessive Congenital Stationary Night Blindness

Published:2010-10 Issue:4 Volume:87 Page:523-531
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Riazuddin S. Amer,Shahzadi Amber,Zeitz Christina,Ahmed Zubair M.,Ayyagari Radha,Chavali Venkata R.M.,Ponferrada Virgilio G.,Audo Isabelle,Michiels Christelle,Lancelot Marie-Elise,Nasir Idrees A.,Zafar Ahmad U.,Khan Shaheen N.,Husnain Tayyab,Jiao Xiaodong,MacDonald Ian M.,Riazuddin Sheikh,Sieving Paul A.,Katsanis Nicholas,Hejtmancik J. Fielding

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

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4. Heterozygous missense mutation in the rhodopsin gene as a cause of congenital stationary night blindness;Dryja;Nat. Genet.,1993

5. Heterozygous missense mutation in the rod cGMP phosphodiesterase beta-subunit gene in autosomal dominant stationary night blindness;Gal;Nat. Genet.,1994

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