Copb2 is essential for embryogenesis and hypomorphic mutations cause human microcephaly
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Title
Copb2 is essential for embryogenesis and hypomorphic mutations cause human microcephaly
Authors
Keywords
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Journal
HUMAN MOLECULAR GENETICS
Volume 26, Issue 24, Pages 4836-4848
Publisher
Oxford University Press (OUP)
Online
2017-09-19
DOI
10.1093/hmg/ddx362
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