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Results: 1
Distribution of deletions and seven point mutations on CYP21B genes in three clinical forms of steroid 21-hydroxylase deficiency.
Authors: Mornet, Etienne Crété, Patrice Kuttenn, Frederique Raux-Demay, Marie-Charles Boué, Joelle White, Perrin C. Boué, Andre
Citation: Mornet, Etienne et al., Distribution of deletions and seven point mutations on CYP21B genes in three clinical forms of steroid 21-hydroxylase deficiency., American journal of human genetics , 48-I(1), 1991, pp. 79-88
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