Two novel mutations found in a patient with 17α-hydroxylase enzyme deficiency

Article

Abstract: Context: Congenital adrenal hyperplasia resulting from 17α- hydroxylase deficiency (17OHD) is a rare

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Autores:

Ergun-Longmire B., New M., Papari-Zareei M., Richard J. Auchus, Tansil S., Wilson R.

Fuentes:

scopus