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Q37385199-926E93C3-8A8C-47D3-ABE8-3B57334D94B2
Q37385199-926E93C3-8A8C-47D3-ABE8-3B57334D94B2
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37385199-926E93C3-8A8C-47D3-ABE8-3B57334D94B2
A novel phenotype related to partial loss of function mutations of the follicle stimulating hormone receptor.
P2860
Q37385199-926E93C3-8A8C-47D3-ABE8-3B57334D94B2
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37385199-926E93C3-8A8C-47D3-ABE8-3B57334D94B2
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Statement
wasDerivedFrom
55f34862c1c501a8b8c9e83630e8e80048b0c5b3
P2860
Clinical features of primary ovarian failure caused by a point mutation in the follicle-stimulating hormone receptor gene