Homozygosity mapping with SNP arrays identifies TRIM32, an E3 ubiquitin ligase, as a Bardet-Biedl syndrome gene (BBS11)-Reference-Cited by-同舟云学术

Homozygosity mapping with SNP arrays identifies TRIM32, an E3 ubiquitin ligase, as a Bardet-Biedl syndrome gene (BBS11)

Published:2006-04-10 Issue:16 Volume:103 Page:6287-6292
ISSN:0027-8424
Container-title:Proceedings of the National Academy of Sciences
language:en
Short-container-title:Proceedings of the National Academy of Sciences

Author:

Chiang A. P.,Beck J. S.,Yen H.-J.,Tayeh M. K.,Scheetz T. E.,Swiderski R. E.,Nishimura D. Y.,Braun T. A.,Kim K.-Y. A.,Huang J.,Elbedour K.,Carmi R.,Slusarski D. C.,Casavant T. L.,Stone E. M.,Sheffield V. C.

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

Reference50 articles.

1. Toward genome-wide SNP genotyping

2. The Cardinal Manifestations of Bardet–Biedl Syndrome, a Form of Laurence–Moon–Biedl Syndrome

3. The Spectrum of Renal Disease in Laurence–Moon–Biedl Syndrome

4. Cardiac abnormalities in the Bardet-Biedl syndrome: Echocardiographic studies of 22 patients

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