Mutations in IFT172 cause isolated retinal degeneration and Bardet–Biedl syndrome
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Title
Mutations in IFT172 cause isolated retinal degeneration and Bardet–Biedl syndrome
Authors
Keywords
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Journal
HUMAN MOLECULAR GENETICS
Volume 24, Issue 1, Pages 230-242
Publisher
Oxford University Press (OUP)
Online
2014-08-29
DOI
10.1093/hmg/ddu441
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