Mutation analysis of phenylketonuria patients from Morocco: high prevalence of mutation G352fsdelG and detection of a novel mutation p.K85X.

Dahri, Saloua

Mutation analysis of phenylketonuria patients from Morocco: high prevalence of mutation G352fsdelG and detection of a novel mutation p.K85X. [electronic resource] - Clinical biochemistry Jan 2010 - 76-81 p. digital

Publication Type: Journal Article; Research Support, Non-U.S. Gov't

1873-2933

10.1016/j.clinbiochem.2009.09.018 doi


DNA Mutational Analysis
Electrophoresis, Polyacrylamide Gel
Genotype
Heterozygote
Humans
Infant
Infant, Newborn
Morocco--epidemiology
Mutation
Phenotype
Phenylalanine Hydroxylase--genetics
Phenylketonurias--epidemiology
Spain