A Case of Combined Oxidative Phosphorylation Deficiency 35 Associated with a Novel Missense Variant of the TRIT1 Gene.
| Autor: | Yıldırım, Miraç, Bektaş, Ömer, Tunçez, Ebru, Yeniay Süt, Nurşah, Sayar, Yavuz, Öncül, Ümmühan, Teber, Serap |
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| Zdroj: | Molecular Syndromology; 2022, Vol. 13 Issue 2, p139-145, 7p |
| Databáze: | Complementary Index |
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