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Whole-exome sequencing identifies recessive WDR62 mutatio... | ResearchHub
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Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations
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Authors
Kaya Bilgüvar
32 more
Kaya Bilgüvar
•
Ali Ozturk
30 more
•
Murat Günel
Published
August 22, 2010
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Journal
Nature
Topics
Biology
Neuroscience
Molecular Biology
Genetics
Mutation
Show all topics
DOI
10.1038/nature09327
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Supporters
Support the authors with ResearchCoin
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Journal
Nature
Topics
Biology
Neuroscience
Molecular Biology
Genetics
Mutation
Show all topics
DOI
10.1038/nature09327
Other Formats
PDF
