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Q24657612-E4A039AA-136E-4F7E-9FB6-F38D16592155
Q24657612-E4A039AA-136E-4F7E-9FB6-F38D16592155
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24657612-E4A039AA-136E-4F7E-9FB6-F38D16592155
Mutations in CHD7, encoding a chromatin-remodeling protein, cause idiopathic hypogonadotropic hypogonadism and Kallmann syndrome
P50
Q24657612-E4A039AA-136E-4F7E-9FB6-F38D16592155
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24657612-E4A039AA-136E-4F7E-9FB6-F38D16592155
rank
NormalRank
type
BestRank
Statement
P1545
2
http://www.w3.org/2001/XMLSchema#string
P1932
Ingo Kurth
http://www.w3.org/2001/XMLSchema#string
P50
Ingo Kurth