Associated Papers
New Genetic Variants in CYP2B6 and SLC6A Support the Role of Oxidative Stress in Familial Ménière's Disease.
Skarp S et al.
Genes, 2022
Histone Modifier Genes Alter Conotruncal Heart Phenotypes in 22q11.2 Deletion Syndrome.
Guo T et al.
American Journal of Human Genetics, 2015
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