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Congenital Adrenal Hyperplasia
The congenital adrenal hyperplasias (CAH) comprise a family of autosomal recessive disorders that disrupt adrenal steroidogenesis. The most common form is due to21-hydroxylase deficiency associated with mutations in the CYP21A2 gene which is located at chromosome 6p21. The clinical features associat...
Αποθηκεύτηκε σε:
| Τόπος έκδοσης: | J Pediatr Adolesc Gynecol |
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| Κύριος συγγραφέας: | |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
2017
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5624825/ https://ncbi.nlm.nih.gov/pubmed/28450075 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jpag.2017.04.001 |
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