TY  - GEN
AU  - Vrzalová,Zuzana
AU  - Hrubá,Zuzana
AU  - St'ahlová Hrabincová,Eva
AU  - Pouchlá,Slavka
AU  - Votava,Felix
AU  - Kolousková,Stanislava
AU  - Fajkusová,Lenka
TI  - Identification of CYP21A2 mutant alleles in Czech patients with 21-hydroxylase deficiency
SN  - 1791-244X
PY  - 2011///0110
KW  - Adrenal Hyperplasia, Congenital
KW  - diagnosis
KW  - Alleles
KW  - Czech Republic
KW  - Gene Deletion
KW  - Gene Duplication
KW  - Genotype
KW  - Humans
KW  - Mutation
KW  - Phenotype
KW  - Point Mutation
KW  - Steroid 21-Hydroxylase
KW  - genetics
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.3892/ijmm_00000504
ER  -