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PROP1 gene mutations in a 36-year-old female presenting with psychosis

SUMMARY: Combined pituitary hormonal deficiency (CPHD) is a rare disease that results from mutations in genes coding for transcription factors that regulate the differentiation of pituitary cells. PROP1 gene mutations are one of the etiological diagnoses of congenital panhypopituitarism, however sym...

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Detalhes bibliográficos
Publicado no:Endocrinol Diabetes Metab Case Rep
Main Authors: Chaudhary, Durgesh Prasad, Rijal, Tshristi, Jha, Kunal Kishor, Saluja, Harpreet
Formato: Artigo
Idioma:Inglês
Publicado em: Bioscientifica Ltd 2017
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5404466/
https://ncbi.nlm.nih.gov/pubmed/28458894
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1530/EDM-16-0096
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