Kwang-Min Sohn
Samsung (South Korea)(KR)Samsung Medical Center(KR)Biomedical Research Institute(US)Sungkyunkwan University(KR)
Publications by Year
Research Areas
Genetic Associations and Epidemiology, Epigenetics and DNA Methylation, Folate and B Vitamins Research, Erythrocyte Function and Pathophysiology, Hereditary Neurological Disorders
Most-Cited Works
- → Mutations in PRPS1, Which Encodes the Phosphoribosyl Pyrophosphate Synthetase Enzyme Critical for Nucleotide Biosynthesis, Cause Hereditary Peripheral Neuropathy with Hearing Loss and Optic Neuropathy (CMTX5)(2007)153 cited
- → A novel missense mutation (I344K) in the SPG4 gene in a Korean family with autosomal-dominant hereditary spastic paraplegia(2002)13 cited
- → Distinct Linkage Disequilibrium (LD) Runs of Single Nucleotide Polymorphisms and Microsatellite Markers; Implications for Use of Mixed Marker Haplotypes in LD-based Mapping(2007)2 cited