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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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Bibliografiske detaljer
Udgivet i:Endocrinol Diabetes Metab Case Rep
Main Authors: Chaudhary, Durgesh Prasad, Rijal, Tshristi, Jha, Kunal Kishor, Saluja, Harpreet
Format: Artigo
Sprog:Inglês
Udgivet: Bioscientifica Ltd 2017
Fag:
Online adgang: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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