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Q37131895-51C0C78B-BDD6-4281-AFAB-820437C9F253
Q37131895-51C0C78B-BDD6-4281-AFAB-820437C9F253
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http://www.wikidata.org/entity/statement/Q37131895-51C0C78B-BDD6-4281-AFAB-820437C9F253
Two coexisting heterozygous frameshift mutations in PROP1 are responsible for a different phenotype of combined pituitary hormone deficiency
P2860
Q37131895-51C0C78B-BDD6-4281-AFAB-820437C9F253
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37131895-51C0C78B-BDD6-4281-AFAB-820437C9F253
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wasDerivedFrom
6abe03bcb27df9f094aefba4a90911a78e36e1ca
P2860
Mutations within the transcription factor PROP1 are rare in a cohort of patients with sporadic combined pituitary hormone deficiency (CPHD).