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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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Detalles Bibliográficos
Autor Principal: Bulun, Serdar E.
Formato: Artigo
Idioma:Inglês
Publicado: 2014
Assuntos:
Acceso en liña: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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