Open AccessFrequency of CYP21 Gene Mutations in Czech Patients with Steroid 21-Hydroxylase Deficiency and Statistical Comparison with Other Populations
Author(s) -
Karel Kotaška,
Richard Průša
Publication year - 2003
Publication title -
medical principles and practice
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.426
H-Index - 45
eISSN - 1423-0151
pISSN - 1011-7571
DOI - 10.1159/000072291
Subject(s) - 21 hydroxylase , medicine , genetics , gene , biology
To undertake mutational analysis in patients with different forms of steroid 21-hydroxylase deficiency.
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