H. Dai

FBXL4 defects are common in patients with congenital lactic acidemia and encephalomyopathic mitochondrial DNA depletion syndrome

W. Craigen, M. Shinawi, A. El-Hattab, 2017, Clinical genetics.

Clinical and molecular spectrum of thymidine kinase 2-related mtDNA maintenance defect.

V. Stefans, Julia Wang, A. El-Hattab, 2018, Molecular genetics and metabolism.