Lourdes R. Desviat
Universidad Autonoma de Madrid Facultad de Ciencias
131 papers found
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Genetic diversity within the R408W phenylketonuria mutation lineages in Europe
UploadFunctional characterization of PCCA mutations causing propionic acidemia
Download from www.researchgate.netMolecular basis of phenylketonuria in Cuba
Download from www.researchgate.netThe Molecular Basis of 3-Methylcrotonylglycinuria, a Disorder of Leucine Catabolism
Download from www.ncbi.nlm.nih.govExpression Analysis of Phenylketonuria Mutations
Download from doi.orgPotential relationship between genotype and clinical outcome in propionic acidaemia patients
Download from www.nature.comThe STR252-IVS10nt546-VNTR7 phenylalanine hydroxylase minihaplotype in five Mediterranean samples.
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