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Article

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

Clinical biochemistry - 1 Jan 2010

Dahri Saloua, Desviat Lourdes R, Pérez Belén, Leal Fátima, Ugarte Magdalena, Chabraoui Layachi

Abstract excerpt

OBJECTIVE: The knowledge of the molecular basis of the Phenylketonuria (PKU, MIM# 261600) in different countries provides relevant information for undertaking specific and rational mutation detection strategies in each population and for the implementation of adequate dietary and cofactor treatment. There are no data available in Moroccan population. DESIGN AND METHODS: In this work we describe the genetic...

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PMID: 19786003
DOI: 10.1016/j.clinbiochem.2009.09.018

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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