Associated Papers
Rare variant genetic landscape of familial chylomicronemia syndrome (FCS) in the United Kingdom.
Bashir B et al.
Genetics in Medicine Open, 2025
40919303 (PubMed )
Supplement: mmc1.pdf
Exome-wide association analysis reveals novel coding sequence variants associated with lipid traits in Chinese.
Tang CS et al.
Nature Communications, 2015
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