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An exceptional Albanian family with seven children presenting with dysmorphic features and mental retardation: maternal phenylketonuria

BACKGROUND: Phenylketonuria is an inborn error of amino acid metabolism which can cause severe damage to the patient or, in the case of maternal phenylketonuria, to the foetus. The maternal phenylketonuria syndrome is caused by high blood phenylalanine concentrations during pregnancy and presents wi...

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Bibliografische gegevens
Hoofdauteurs: Knerr, Ina, Zschocke, Johannes, Schellmoser, Stefan, Topf, Hans G, Weigel, Corina, Dötsch, Jörg, Rascher, Wolfgang
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: BioMed Central 2005
Onderwerpen:
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC1079877/
https://ncbi.nlm.nih.gov/pubmed/15811181
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2431-5-5
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