Mutations in SPATA7 Cause Leber Congenital Amaurosis and Juvenile Retinitis Pigmentosa-Reference-Cited by-同舟云学术

Mutations in SPATA7 Cause Leber Congenital Amaurosis and Juvenile Retinitis Pigmentosa

Published:2009-03 Issue:3 Volume:84 Page:380-387
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Wang Hui,den Hollander Anneke I.,Moayedi Yalda,Abulimiti Abuduaini,Li Yumei,Collin Rob W.J.,Hoyng Carel B.,Lopez Irma,Bray Molly,Lewis Richard Alan,Lupski James R.,Mardon Graeme,Koenekoop Robert K.,Chen Rui

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference36 articles.

1. Uber retinitis pigmentosa und angeborene amaurose;Leber;Albrecht Von Graefes Arch. Ophthalmol.,1869

2. Mutational analysis and clinical correlation in Leber congenital amaurosis;Dharmaraj;Ophthalmic Genet.,2000

3. Juvenile Hereditary Macular Dystrophies;Lewis,1988

4. Leber congenital amaurosis and retinitis pigmentosa with Coats-like exudative vasculopathy are associated with mutations in the crumbs homologue 1 (CRB1) gene;den Hollander;Am. J. Hum. Genet.,2001

5. De novo mutations in the CRX homeobox gene associated with Leber congenital amaurosis;Freund;Nat. Genet.,1998

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