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Q37131895-E9251BAF-C57D-44E0-9984-7E9DC891ED97
Q37131895-E9251BAF-C57D-44E0-9984-7E9DC891ED97
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Statement
http://www.wikidata.org/entity/statement/Q37131895-E9251BAF-C57D-44E0-9984-7E9DC891ED97
Two coexisting heterozygous frameshift mutations in PROP1 are responsible for a different phenotype of combined pituitary hormone deficiency
P2860
Q37131895-E9251BAF-C57D-44E0-9984-7E9DC891ED97
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37131895-E9251BAF-C57D-44E0-9984-7E9DC891ED97
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wasDerivedFrom
6abe03bcb27df9f094aefba4a90911a78e36e1ca
P2860
Prolonged jaundice and hypothyroidism as the presenting symptoms in a neonate with a novel Prop1 gene mutation (Q83X).