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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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Библиографические подробности
Опубликовано в: :Endocrinol Diabetes Metab Case Rep
Главные авторы: Chaudhary, Durgesh Prasad, Rijal, Tshristi, Jha, Kunal Kishor, Saluja, Harpreet
Формат: Artigo
Язык:Inglês
Опубликовано: Bioscientifica Ltd 2017
Предметы:
Online-ссылка: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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