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A framework for the interpretation of de novo mutation in... | ResearchHub
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A framework for the interpretation of de novo mutation in human disease
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Authors
Kaitlin Samocha
27 more
Kaitlin Samocha
•
Elise Robinson
25 more
•
Mark Daly
Published
August 3, 2014
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Journal
Nature Genetics
Topics
Biology
Genetics
Molecular Biology
Phenotype
Loss Function
Show all topics
DOI
10.1038/ng.3050
Other Formats
PDF
Supporters
Support the authors with ResearchCoin
Tip RSC
Journal
Nature Genetics
Topics
Biology
Genetics
Molecular Biology
Phenotype
Loss Function
Show all topics
DOI
10.1038/ng.3050
Other Formats
PDF
