2023
DOI: 10.1016/j.genrep.2023.101819
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Novel missense mutation in NKX2.6 gene (c.389 G > C, Arg130Pro) as a potentially pathogenic variant in pediatric patients with congenital heart disease

Mehri Khatami,
Donya Ghazinader,
Fatemeh Ahmadi
et al.
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