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(2023) Novel missense mutation in<i> NKX2.6</i> gene (c.389 G > C, Arg130Pro) as a potentially pathogenic variant in pediatric patients with congenital heart disease. Gene Reports. p. 10.
(2022) Mitochondrial Mutations in Protein Coding Genes of Respiratory Chain Including Complexes Iv, V, And Mt-Trna Genes Are Associated Risk Factors for Congenital Heart Disease. EXCLI Journal. pp. 1306-1330.