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Q37131895-CE713DA1-1877-4748-92A3-4823AC4000B0
Q37131895-CE713DA1-1877-4748-92A3-4823AC4000B0
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http://www.wikidata.org/entity/statement/Q37131895-CE713DA1-1877-4748-92A3-4823AC4000B0
Two coexisting heterozygous frameshift mutations in PROP1 are responsible for a different phenotype of combined pituitary hormone deficiency
P2860
Q37131895-CE713DA1-1877-4748-92A3-4823AC4000B0
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37131895-CE713DA1-1877-4748-92A3-4823AC4000B0
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6abe03bcb27df9f094aefba4a90911a78e36e1ca
P2860
Pituitary magnetic resonance imaging in 15 patients with Prop1 gene mutations: pituitary enlargement may originate from the intermediate lobe.