Mutations in a BTB-Kelch Protein, KLHL7, Cause Autosomal-Dominant Retinitis Pigmentosa-Reference-Cited by-同舟云学术

Mutations in a BTB-Kelch Protein, KLHL7, Cause Autosomal-Dominant Retinitis Pigmentosa

Published:2009-06 Issue:6 Volume:84 Page:792-800
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Friedman James S.,Ray Joseph W.,Waseem Naushin,Johnson Kory,Brooks Matthew J.,Hugosson Therése,Breuer Debra,Branham Kari E.,Krauth Daniel S.,Bowne Sara J.,Sullivan Lori S.,Ponjavic Vesna,Gränse Lotta,Khanna Ritu,Trager Edward H.,Gieser Linn M.,Hughbanks-Wheaton Dianna,Cojocaru Radu I.,Ghiasvand Noor M.,Chakarova Christina F.,Abrahamson Magnus,Göring Harald H.H.,Webster Andrew R.,Birch David G.,Abecasis Goncalo R.,Fann Yang,Bhattacharya Shomi S.,Daiger Stephen P.,Heckenlively John R.,Andréasson Sten,Swaroop Anand

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

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