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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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| Published in: | Endocrinol Diabetes Metab Case Rep |
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| Main Authors: | , , , |
| Format: | Artigo |
| Language: | Inglês |
| Published: |
Bioscientifica Ltd
2017
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| Subjects: | |
| Online Access: | 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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