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AROMATASE DEFICIENCY

Studies on the phenotypes of women and men with mutations disrupting estrogen biosynthesis and action significantly advanced our knowledge of the physiologic roles of estrogen in humans. Aromatase deficiency results from autosomal recessive inheritance of mutations in the CYP19A1 gene. It gives rise...

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Bibliographic Details
Main Author: Bulun, Serdar E.
Format: Artigo
Language:Inglês
Published: 2014
Subjects:
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC3939057/
https://ncbi.nlm.nih.gov/pubmed/24485503
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.fertnstert.2013.12.022
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