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Genetic Analysis in Patients With Kallmann Syndrome: Coexistence of Mutations in Prokineticin Receptor 2 and KAL1

✍ Scribed by Canto, P.; Munguia, P.; Soderlund, D.; Castro, J. J.; Mendez, J. P.

Book ID: 119924687
Publisher: American Society of Andrology
Year: 2008
Tongue: English
Weight: 434 KB
Volume: 30
Category: Article
ISSN: 1939-4640
DOI: 10.2164/jandrol.108.005314

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