A Truncated Form of Rod Photoreceptor PDE6 β-Subunit Causes Autosomal Dominant Congenital Stationary Night Blindness by Interfering with the Inhibitory Activity of the γ-Subunit-Reference-Cited by-同舟云学术

A Truncated Form of Rod Photoreceptor PDE6 β-Subunit Causes Autosomal Dominant Congenital Stationary Night Blindness by Interfering with the Inhibitory Activity of the γ-Subunit

Published:2014-04-23 Issue:4 Volume:9 Page:e95768
ISSN:1932-6203
Container-title:PLoS ONE
language:en
Short-container-title:PLoS ONE

Author:

Manes Gaël,Cheguru Pallavi,Majumder Anurima,Bocquet Béatrice,Sénéchal Audrey,Artemyev Nikolai O.,Hamel Christian P.,Brabet Philippe

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

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

5. Two-site high-affinity interaction between inhibitory and catalytic subunits of rod cyclic GMP phosphodiesterase;NO Artemyev;Biochem J 283 (Pt,1992

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