Mutations in CABP4, the Gene Encoding the Ca2+-Binding Protein 4, Cause Autosomal Recessive Night Blindness-Reference-Cited by-同舟云学术

Mutations in CABP4, the Gene Encoding the Ca2+-Binding Protein 4, Cause Autosomal Recessive Night Blindness

Published:2006-10 Issue:4 Volume:79 Page:657-667
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Zeitz Christina,Kloeckener-Gruissem Barbara,Forster Ursula,Kohl Susanne,Magyar István,Wissinger Bernd,Mátyás Gábor,Borruat François-Xavier,Schorderet Daniel F.,Zrenner Eberhart,Munier Francis L.,Berger Wolfgang

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference38 articles.

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3. A novel mutation within the rhodopsin gene (Thr-94-Ile) causing autosomal dominant congenital stationary night blindness;al Jandal;Hum Mutat,1999

4. Missense mutation in the gene encoding the alpha subunit of rod transducin in the Nougaret form of congenital stationary night blindness;Dryja;Nat Genet,1996

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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