Associated Papers
Novel mutation of transferrin receptor 2 causing hereditary hemochromatosis type 3 in a Japanese patient.
Tamai Y et al.
Hepatology Research : the Official Journal of the Japan Society of Hepatology, 2024
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
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