A novel loss-of-function mutation in Npr2 clarifies primary role in female reproduction and reveals a potential therapy for acromesomelic dysplasia, Maroteaux type

Title
A novel loss-of-function mutation in Npr2 clarifies primary role in female reproduction and reveals a potential therapy for acromesomelic dysplasia, Maroteaux type
Authors
Keywords
-
Journal
HUMAN MOLECULAR GENETICS
Volume 22, Issue 2, Pages 345-357
Publisher
Oxford University Press (OUP)
Online
2012-10-14
DOI
10.1093/hmg/dds432

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