Transgenic mice carrying theH258N mutation in the gene encoding the β-subunit of phosphodiesterase-6 (PDE6B) provide a model for human congenital stationary night blindness-Reference-Cited by-同舟云学术

Transgenic mice carrying theH258N mutation in the gene encoding the β-subunit of phosphodiesterase-6 (PDE6B) provide a model for human congenital stationary night blindness

Published:2007 Issue:3 Volume:28 Page:243-254
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Tsang Stephen H.,Woodruff Michael L.,Jun Lin,Mahajan Vinit,Yamashita Clyde K.,Pedersen Robert,Lin Chyuan-Sheng,Goff Stephen P.,Rosenberg Thomas,Larsen Michael,Farber Debora B.,Nusinowitz Steven

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference82 articles.

1. Noncatalytic cGMP-binding sites of amphibian rod cGMP phosphodiesterase control interaction with its inhibitory gamma-subunits. A putative regulatory mechanism of the rod photoresponse.

2. G Proteins and Phototransduction

3. The Knockout Mouse Project

4. Isolation and characterization of cGMP phosphodiesterase from bovine rod outer segments.

5. 1978. Phylogenetic analysis. In: editor. Origins of inbred mice. New York: Academic Press: Wiley-Interscience. 15p.

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