A Case of Combined Oxidative Phosphorylation Deficiency 35 Associated with a Novel Missense Variant of the < b > < i > TRIT1 < /i > < /b > Gene

This study expands the genotype-phenotype spectrum ofTRIT1-related COXPD35.Mol Syndromol
Source: Molecular Syndromology - Category: Molecular Biology Source Type: research