TY  - GEN
AU  - Abid,Fatima
AU  - Tardy,Véronique
AU  - Gaouzi,Ahmed
AU  - El Hessni,Aboubaker
AU  - Morel,Yves
AU  - Chabraoui,Layachi
TI  - CYP21A2 gene mutation analysis in Moroccan patients with classic form of 21-hydroxylase deficiency: high regional prevalence of p.Q318X mutation and identification of a novel p.L353R mutation
SN  - 1434-6621
PY  - 2009///0324
KW  - Adrenal Hyperplasia, Congenital
KW  - genetics
KW  - Child, Preschool
KW  - Female
KW  - Genotype
KW  - Humans
KW  - Infant
KW  - Infant, Newborn
KW  - Male
KW  - Morocco
KW  - Mutation
KW  - Steroid 21-Hydroxylase
N1  - Publication Type: Journal Article
UR  - https://doi.org/10.1515/CCLM.2008.339
ER  -