Autosomal-Dominant Retinitis Pigmentosa Caused by a Mutation in SNRNP200, a Gene Required for Unwinding of U4/U6 snRNAs-Reference-Cited by-同舟云学术

Autosomal-Dominant Retinitis Pigmentosa Caused by a Mutation in SNRNP200, a Gene Required for Unwinding of U4/U6 snRNAs

Published:2009-11 Issue:5 Volume:85 Page:617-627
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Zhao Chen,Bellur Deepti L.,Lu Shasha,Zhao Feng,Grassi Michael A.,Bowne Sara J.,Sullivan Lori S.,Daiger Stephen P.,Chen Li Jia,Pang Chi Pui,Zhao Kanxing,Staley Jonathan P.,Larsson Catharina

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference54 articles.

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4. A human homolog of yeast pre-mRNA splicing gene, PRP31, underlies autosomal dominant retinitis pigmentosa on chromosome 19q13.4 (RP11);Vithana;Mol. Cell,2001

5. Mutations in HPRP3, a third member of pre-mRNA splicing factor genes, implicated in autosomal dominant retinitis pigmentosa;Chakarova;Hum. Mol. Genet.,2002

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