WorldCat Link Resolver, the OpenURL link-server from OCLC

Mutations in the CEP290 %28NPHP6%29 gene are a frequent caus…

Mutations in the CEP290 %28NPHP6%29 gene are a frequent cause of Leber congenital amaurosis.

Article, Chapter

Authors: A.I. den Hollander

Publication: American Journal of Human Genetics, The, Volume:79, Issue:3, Page(s):556-561

Published: Cell Press, 2006

ISSN: 0002-9297

Full text availability for this item

View Full Text Source:American Journal of Human Genetics, The,American Journal of Human Genetics, The,Elsevier ScienceDirect Journals Opens in new Window

Journal: American Journal of Human Genetics, The Source:Elsevier ScienceDirect Journals Opens in new Window

Collection: Elsevier ScienceDirect Journals Opens in new Window

Coverage:

1997-06~present; volume:60~present;issue:6~present

View Full Text Source:American Journal of Human Genetics, The,American Journal of Human Genetics, The,Cell Press Opens in new Window

Journal: American Journal of Human Genetics, The Source:Cell Press Opens in new Window

Collection: Cell Press Opens in new Window

Coverage:

1997-06~present; volume:60~present;issue:6~present

View Full Text Source:American Journal of Human Genetics,American Journal of Human Genetics,PubMed Central Opens in new Window

Journal: American Journal of Human Genetics Source:PubMed Central Opens in new Window

Collection: PubMed Central Opens in new Window

Coverage:

1949~6 months ago; volume:1~6 months ago

Browse related articles

Print copies at your library

Check availability in RUQuest

Request a copy of this item

Cite this item