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Q30442563-6205E31B-CCCD-4B6C-A011-2D3ED3A0775D
Q30442563-6205E31B-CCCD-4B6C-A011-2D3ED3A0775D
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Statement
http://www.wikidata.org/entity/statement/Q30442563-6205E31B-CCCD-4B6C-A011-2D3ED3A0775D
Loss-of-function mutation in the prokineticin 2 gene causes Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism
P2860
Q30442563-6205E31B-CCCD-4B6C-A011-2D3ED3A0775D
BestRank
Statement
http://www.wikidata.org/entity/statement/Q30442563-6205E31B-CCCD-4B6C-A011-2D3ED3A0775D
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wasDerivedFrom
e08859917868d9d0507d45a6512568c4aab9d9b0
P2860
The candidate gene for the X-linked Kallmann syndrome encodes a protein related to adhesion molecules