Direct genomic PCR sequencing of the high affinity thiamine transporter (SLC19A2) gene identifies three genetic variants in Wernicke Korsakoff syndrome (WKS)

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Bibliographische Detailangaben
Veröffentlicht in:	American journal of medical genetics. Part B, Neuropsychiatric genetics Neuropsychiatric genetics, 2005-08, Vol.137B (1), p.17-19
Hauptverfasser:	Guerrini, Irene, Thomson, Allan D., Cook, Cristopher C.H., McQuillin, Andrew, Sharma, Vishal, Kopelman, Michael, Reynolds, Gerald, Jauhar, Pramod, Harper, Clive, Gurling, Hugh M.D.
Format:	Artikel
Sprache:	eng
Schlagworte:	alcoholism Alcoholism - complications DNA - chemistry DNA - genetics DNA Mutational Analysis - methods Exons - genetics Female Humans Korsakoff Syndrome - etiology Korsakoff Syndrome - genetics Male Membrane Transport Proteins - genetics Middle Aged Mutation mutation analysis Point Mutation Polymerase Chain Reaction - methods Polymorphism, Genetic Sequence Deletion thiamine deficiency thiamine transport
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