Mutations in IFT172 cause isolated retinal degeneration and Bardet–Biedl syndrome-Reference-Cited by-同舟云学术

Mutations in IFT172 cause isolated retinal degeneration and Bardet–Biedl syndrome

Published:2014-08-28 Issue:1 Volume:24 Page:230-242
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Bujakowska Kinga M.,Zhang Qi,Siemiatkowska Anna M.,Liu Qin,Place Emily,Falk Marni J.,Consugar Mark,Lancelot Marie-Elise,Antonio Aline,Lonjou Christine,Carpentier Wassila,Mohand-Saïd Saddek,den Hollander Anneke I.,Cremers Frans P.M.,Leroy Bart P.,Gai Xiaowu,Sahel José-Alain,van den Born L. Ingeborgh,Collin Rob W.J.,Zeitz Christina,Audo Isabelle,Pierce Eric A.

Publisher

Oxford University Press (OUP)

Subject

Genetics(clinical),Genetics,Molecular Biology,General Medicine

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4. Mutations in a gene encoding a new oxygen-regulated photoreceptor protein cause dominant retinitis pigmentosa;Nat. Genet.,1999

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