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...
| Päätekijät: | , , , , , , , |
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| Aineistotyyppi: | Artikkeli |
| Kieli: | English |
| Julkaistu: |
Brazilian Society of Endocrinology and Metabolism
2016-10-01
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| Sarja: | Archives of Endocrinology and Metabolism |
| Linkit: | http://www.scielo.br/scielo.php?script=sci_arttext&pid=S2359-39972016000500500&lng=en&tlng=en |