Associated Papers
Exome sequencing and analysis of 454,787 UK Biobank participants.
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Nature, 2021
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Supplement: 41586_2021_4103_MOESM4_ESM.xlsx › ST6
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
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Supplement: 10072_2020_4876_MOESM3_ESM.xlsx › variants
Germline Mutation in MUS81 Resulting in Impaired Protein Stability is Associated with Familial Breast and Thyroid Cancer.
Pinheiro M et al.
Cancers, 2020
32443704 (PubMed )
Supplement: cancers-12-01289-s001.zip › cancers-768495_-Supplementary_Tables_.xlsx › Table_S2
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