Mutations in SDCCAG8/NPHP10 Cause Bardet-Biedl Syndrome and Are Associated with Penetrant Renal Disease and Absent Polydactyly-Reference-Cited by-同舟云学术

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Mutations in SDCCAG8/NPHP10 Cause Bardet-Biedl Syndrome and Are Associated with Penetrant Renal Disease and Absent Polydactyly

Published:2010 Issue:6 Volume:1 Page:273-281
ISSN:1661-8769
Container-title:Molecular Syndromology
language:en
Short-container-title:Mol Syndromol

Author:

Schaefer E.,Zaloszyc A.,Lauer J.,Durand M.,Stutzmann F.,Perdomo-Trujillo Y.,Redin C.,Bennouna Greene V.,Toutain A.,Perrin L.,Gérard M.,Caillard S.,Bei X.,Lewis R.A.,Christmann D.,Letsch J.,Kribs M.,Mutter C.,Muller J.,Stoetzel C.,Fischbach M.,Marion V.,Katsanis N.,Dollfus H.

Publisher

S. Karger AG

Subject

Genetics (clinical),Genetics

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