Mutations in LRP5 or FZD4 Underlie the Common Familial Exudative Vitreoretinopathy Locus on Chromosome 11q-Reference-Cited by-同舟云学术

Mutations in LRP5 or FZD4 Underlie the Common Familial Exudative Vitreoretinopathy Locus on Chromosome 11q

Published:2004-04 Issue:4 Volume:74 Page:721-730
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Toomes Carmel,Bottomley Helen M.,Jackson Richard M.,Towns Katherine V.,Scott Sheila,Mackey David A.,Craig Jamie E.,Jiang Li,Yang Zhenglin,Trembath Richard,Woodruff Geoffrey,Gregory-Evans Cheryl Y.,Gregory-Evans Kevin,Parker Michael J.,Black Graeme C.M.,Downey Louise M.,Zhang Kang,Inglehearn Chris F.

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

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