R339H and P453S: CYP21 mutations associated with nonclassic...

Molecular Endocrinology 1992 / 08 Vol. 6; Iss. 8

R339H and P453S: CYP21 mutations associated with nonclassic steroid 21-hydroxylase deficiency that are not apparent gene conversions.

Helmberg, A, Tusie-Luna, M T, Tabarelli, M, Kofler, R, White, P C
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Volume:
6
Language:
english
Journal:
Molecular Endocrinology
DOI:
10.1210/mend.6.8.1406709
Date:
August, 1992
File:
PDF, 791 KB
english, 1992
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