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Journals and Conferences
Recessive mutations of SLC26A4 (PDS) are a common cause of Pendred syndrome and non-syndromic deafness in western populations. Although south and east Asia contain nearly one half of the global… (More)
In Japanese, Koreans and Caucasians, narcolepsy/hypocretin deficiency is tightly associated with the DRB1*15:01-DQA1*01:02-DQB1*06:02 haplotype. Studies in African-Americans suggest a primary effect… (More)
The minor allele of a single nucleotide polymorphism (SNP) in the PTPN22 gene (1858T) encoding the Lyp-tyrosine phosphatase has been recently associated with multiple autoimmune disorders, raising… (More)
A new HLA-B*52 allele differs from B*52:01:01 by a single nucleotide exchange at position 583 where a 'C' to 'T'.
Identification of a novel human leukocyte antigen-B allele HLA-B*4070.
The novel HLA (human leukocyte angiten)-A*26 allele differs from A*26:01:01 by a single nucleotide substitution at position 292 of exon 2 where a 'G' change to 'C'.
The HLA-B*40:74 allele has two nucleotide changes at positions 103 and 106 of exon 2 from the closest matching allele HLA-B*40:01:01.