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A common allele in RPGRIP1L is a modifier of retinal dege... | ResearchHub
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A common allele in RPGRIP1L is a modifier of retinal degeneration in ciliopathies
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Authors
Hemant Khanna
33 more
Hemant Khanna
•
Colin Johnson
31 more
•
Nicholas Katsanis
Published
May 10, 2009
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Journal
Nature Genetics
Topics
Biology
Genetics
Molecular Biology
Phenotype
Retinitis Pigmentosa
Show all topics
DOI
10.1038/ng.366
Other Formats
PDF
Supporters
Support the authors with ResearchCoin
Tip RSC
Journal
Nature Genetics
Topics
Biology
Genetics
Molecular Biology
Phenotype
Retinitis Pigmentosa
Show all topics
DOI
10.1038/ng.366
Other Formats
PDF
