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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...
Tallennettuna:
| Päätekijä: | |
|---|---|
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
2014
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| Aiheet: | |
| Linkit: | 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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