Long-term follow-up of a female with congenital adrenal hyperplasia due to P450-oxidoreductase deficiency
SUMMARY P450 oxidoreductase deficiency (PORD) is a variant of congenital adrenal hyperplasia that is caused by POR gene mutations. The POR gene encodes a flavor protein that transfers electrons from nicotinamide adenine dinucleotide phosphate (NADPH) to all microsomal cytochrome P450 type II (includ...
| Những tác giả chính: | , , , , , , , |
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| Định dạng: | Bài viết |
| Ngôn ngữ: | English |
| Được phát hành: |
Brazilian Society of Endocrinology and Metabolism
2016-10-01
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| Loạt: | Archives of Endocrinology and Metabolism |
| Truy cập trực tuyến: | http://www.scielo.br/scielo.php?script=sci_arttext&pid=S2359-39972016000500500&lng=en&tlng=en |