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Exome sequencing in sporadic autism spectrum disorders id... | ResearchHub
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Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations
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Authors
Brian O’Roak
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Brian O’Roak
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Pelagia Deriziotis
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Evan Eichler
Published
May 15, 2011
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Journal
Nature Genetics
Topics
Biology
Epidemiology
Medicine
Cognitive Neuroscience
Phenotype
Show all topics
DOI
10.1038/ng.835
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Supporters
Support the authors with ResearchCoin
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Journal
Nature Genetics
Topics
Biology
Epidemiology
Medicine
Cognitive Neuroscience
Phenotype
Show all topics
DOI
10.1038/ng.835
Other Formats
PDF
