1.
H28+C insertion in the CYP21 gene: A novel frameshift mutation in a brazilian patient with the classical form of 21-hydroxylase deficiency
by LAU, Ivy F
The journal of clinical endocrinology and metabolism, 2001, Vol.86 (12), p.5877-5880
2.
CYP21 mutations in simple virilizing congenital adrenal hyperplasia
by LAJIC, Svetlana
Journal of molecular medicine (Berlin, Germany), 2001, Vol.79 (10), p.581-586
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