Associated Papers
Whole-exome sequencing in patients with protein aggregate myopathies reveals causative mutations associated with novel atypical phenotypes.
Machnicki MM et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 2021
33170376 (PubMed )
Supplement: 10072_2020_4876_MOESM3_ESM.xlsx › variants
Identification of novel non-synonymous variants associated with type 2 diabetes-related metabolites in Korean population.
Park TJ et al.
Bioscience Reports, 2019
31652446 (PubMed )
Supplement: BSR-2019-0078_supp.pdf
Identification of 12 novel loci that confer susceptibility to early-onset dyslipidemia.
Yamada Y et al.
International Journal of Molecular Medicine, 2019
Identification of eight genetic variants as novel determinants of dyslipidemia in Japanese by exome-wide association studies.
Yamada Y et al.
Oncotarget, 2017
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