Associated Papers
High prevalence of deleterious mutations in concomitant nonsyndromic cleft and outflow tract heart defects.
Munabi NCO et al.
American Journal of Medical Genetics. Part A, 2022
Global genetic diversity of human apolipoproteins and effects on cardiovascular disease risk.
Zhou Y et al.
Journal of Lipid Research, 2018
30076208 (PubMed )
Supplement: 10.1194_P086710_jlr.P086710-4.xlsx › APOB
Whole exome sequencing identification of novel candidate genes in patients with proliferative diabetic retinopathy.
Ung C et al.
Vision Research, 2017
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