Associated Papers
Genome-wide rare variant analysis for thousands of phenotypes in over 70,000 exomes from two cohorts.
Cirulli ET et al.
Nature Communications, 2020
31992710 (PubMed )
Supplement: 41467_2020_14288_MOESM1_ESM.pdf
A new apolipoprotein Al variant, Trp50Arg, causes hereditary amyloidosis.
Booth DR et al.
Qjm : Monthly Journal of the Association of Physicians, 1995
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