Mutation screening of SEMA3A and SEMA7A in patients with congenital hypogonadotropic hypogonadism
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Title
Mutation screening of SEMA3A and SEMA7A in patients with congenital hypogonadotropic hypogonadism
Authors
Keywords
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Journal
PEDIATRIC RESEARCH
Volume 75, Issue 5, Pages 641-644
Publisher
Springer Nature
Online
2014-02-13
DOI
10.1038/pr.2014.23
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- Reversible Congenital Hypogonadotropic Hypogonadism in Patients with CHD7, FGFR1 or GNRHR Mutations
- (2012) Eeva-Maria Laitinen et al. PLoS One
- SEMA3A, a Gene Involved in Axonal Pathfinding, Is Mutated in Patients with Kallmann Syndrome
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