Leber Congenital Amaurosis and Retinitis Pigmentosa with Coats-like Exudative Vasculopathy Are Associated with Mutations in the Crumbs Homologue 1 (CRB1) Gene-Reference-Cited by-同舟云学术

Leber Congenital Amaurosis and Retinitis Pigmentosa with Coats-like Exudative Vasculopathy Are Associated with Mutations in the Crumbs Homologue 1 (CRB1) Gene

Published:2001-07 Issue:1 Volume:69 Page:198-203
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Hollander Anneke I. den,Heckenlively John R.,van den Born L. Ingeborgh,de Kok Yvette J.M.,van der Velde-Visser Saskia D.,Kellner Ulrich,Jurklies Bernhard,van Schooneveld Mary J.,Blankenagel Anita,Rohrschneider Klaus,Wissinger Bernd,Cruysberg Johan R.M.,Deutman August F.,Brunner Han G.,Apfelstedt-Sylla Eckart,Hoyng Carel B.,Cremers Frans P.M.

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference22 articles.

1. Mutations in a human homologue of Drosophila crumbs cause retinitis pigmentosa (RP12);den Hollander;Nat Genet,1999

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

3. Classification of congenital and early onset retinitis pigmentosa;Foxman;Arch Ophthalmol,1985

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

5. Mutations in RPE65 cause autosomal recessive childhood-onset severe retinal dystrophy;Gu;Nat Genet,1997

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