Associated Papers
Extensive disruption of protein interactions by genetic variants across the allele frequency spectrum in human populations.
Fragoza R et al.
Nature Communications, 2019
31515488 (PubMed )
Supplement: 41467_2019_11959_MOESM11_ESM.xlsx › SD7_-_Drug_Targets
Association between SNPs and haplotypes in the METTL21C gene and peak bone mineral density and body composition in Chinese male nuclear families.
Zhao F et al.
Journal of Bone and Mineral Metabolism, 2017
Mutations in the histamine N-methyltransferase gene, HNMT, are associated with nonsyndromic autosomal recessive intellectual disability.
Heidari A et al.
Human Molecular Genetics, 2015
Lysine methylation of VCP by a member of a novel human protein methyltransferase family.
Kernstock S et al.
Nature Communications, 2012
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