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Identification of FOXP2 Truncation as a Novel Cause of De... | ResearchHub
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Identification of FOXP2 Truncation as a Novel Cause of Developmental Speech and Language Deficits
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Authors
K MacDermot
10 more
K MacDermot
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Elena Bonora
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•
Simon Fisher
Published
May 6, 2005
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Journal
The American Journal of Human Genetics
Topics
Biology
Neuroscience
Molecular Biology
Developmental And Educational Psychology
Genetics
Show all topics
DOI
10.1086/430841
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publisher-specific-oa
Supporters
Support the authors with ResearchCoin
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Journal
The American Journal of Human Genetics
Topics
Biology
Neuroscience
Molecular Biology
Developmental And Educational Psychology
Genetics
Show all topics
DOI
10.1086/430841
License
publisher-specific-oa
