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Mutations in the CEP290 (NPHP6) Gene Are a Frequent Cause... | ResearchHub
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Mutations in the CEP290 (NPHP6) Gene Are a Frequent Cause of Leber Congenital Amaurosis
0
Authors
Anneke Hollander
13 more
Anneke Hollander
•
Krysta Voesenek
11 more
•
Frans Cremers
Published
August 8, 2006
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Journal
The American Journal of Human Genetics
Topics
Biology
Medicine
Molecular Biology
Mutation
Genetics
Show all topics
DOI
10.1086/507318
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publisher-specific-oa
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Journal
The American Journal of Human Genetics
Topics
Biology
Medicine
Molecular Biology
Mutation
Genetics
Show all topics
DOI
10.1086/507318
License
publisher-specific-oa
