PROKR2 missense mutations associated with Kallmann syndrome impair receptor signalling activity

Published 2008 View Full Article

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Title
PROKR2 missense mutations associated with Kallmann syndrome impair receptor signalling activity
Authors
Keywords
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Journal
HUMAN MOLECULAR GENETICS
Volume 18, Issue 1, Pages 75-81
Publisher
Oxford University Press (OUP)
Online
2008-10-01
DOI
10.1093/hmg/ddn318
References
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