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The KAL1 pVal610Ile mutation is a recessive mutation causing Kallmann syndrome

✍ Scribed by Zhang, Shilin; Xu, Hao; Wang, Tao; Liu, Guoqing; Liu, Jihong

Book ID: 120431291
Publisher: Elsevier Science
Year: 2013
Tongue: English
Weight: 406 KB
Volume: 99
Category: Article
ISSN: 1556-5653
DOI: 10.1016/j.fertnstert.2013.01.099

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