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Q34139361-6C282266-16A3-4D6C-B2C0-9E3DE6C7B245
Q34139361-6C282266-16A3-4D6C-B2C0-9E3DE6C7B245
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http://www.wikidata.org/entity/statement/Q34139361-6C282266-16A3-4D6C-B2C0-9E3DE6C7B245
A Hypomorphic Allele in the FGF8 Gene Contributes to Holoprosencephaly and Is Allelic to Gonadotropin-Releasing Hormone Deficiency in Humans
P2860
Q34139361-6C282266-16A3-4D6C-B2C0-9E3DE6C7B245
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34139361-6C282266-16A3-4D6C-B2C0-9E3DE6C7B245
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wasDerivedFrom
90209dc9897a818483fb4dcfe810d14fb6ab02bf
P2860
The mutational spectrum of holoprosencephaly-associated changes within the SHH gene in humans predicts loss-of-function through either key structural alterations of the ligand or its altered synthesis.