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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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References
2005
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Genetic VariantsMendelian DisorderWernicke Korsakoff SyndromeGenetic DisorderGeneticsInherited Metabolic DiseaseMolecular GeneticsGene Identifies ThreeDisease Gene IdentificationSystems BiologyMedicineClinical Genetics
| Year | Citations | |
|---|---|---|
1982 | 797 | |
1983 | 567 | |
1977 | 396 | |
1982 | 341 | |
1999 | 204 | |
1995 | 121 | |
Cloning of human transketolase cDNAs and comparison of the nucleotide sequence of the coding region in Wernicke-Korsakoff and non-Wernicke-Korsakoff individuals. Brian A. McCool, Steven G. Plonk, Peter Martin, Journal of Biological Chemistry GeneticsMolecular BiologyPathologyGene CharacterizationMolecular Genetics | 1993 | 77 |
1989 | 68 | |
2002 | 62 | |
2003 | 33 |
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