TY  - GEN
AU  - Dahri,Saloua
AU  - Desviat,Lourdes R
AU  - Pérez,Belén
AU  - Leal,Fátima
AU  - Ugarte,Magdalena
AU  - Chabraoui,Layachi
TI  - Mutation analysis of phenylketonuria patients from Morocco: high prevalence of mutation G352fsdelG and detection of a novel mutation p.K85X
SN  - 1873-2933
PY  - 2010///0330
KW  - DNA Mutational Analysis
KW  - Electrophoresis, Polyacrylamide Gel
KW  - Genotype
KW  - Heterozygote
KW  - Humans
KW  - Infant
KW  - Infant, Newborn
KW  - Morocco
KW  - epidemiology
KW  - Mutation
KW  - Phenotype
KW  - Phenylalanine Hydroxylase
KW  - genetics
KW  - Phenylketonurias
KW  - Spain
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1016/j.clinbiochem.2009.09.018
ER  -