Associated Papers
Whole genome deep sequencing analysis of cell-free DNA in samples with low tumour content.
Ganesamoorthy D et al.
Bmc Cancer, 2022
35057759 (PubMed )
Supplement: 12885_2021_9160_MOESM1_ESM.xlsx › 065_P0
Low-Frequency and Rare-Coding Variation Contributes to Multiple Sclerosis Risk.
Unknown Author
Cell, 2018
Mutations in SLC39A14 disrupt manganese homeostasis and cause childhood-onset parkinsonism-dystonia.
Tuschl K et al.
Nature Communications, 2016
27231142 (PubMed )
Supplement: ncomms11601-s1.pdf
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