Amit VATKAR; S. Joshi NISHIGANDHA; Smita PATIL; Mumtaz SHARIFF. Novel HADHA Mutation Causes Mitochondrial Protein Deficiency and Neuromuscular Disease. Advanced Concepts in Medicine and Medical Research Vol. 11, [S. l.], p. 74–78, 2023. DOI: 10.9734/bpi/acmmr/v11/7030E. Disponível em: https://stm.bookpi.org/ACMMR-V11/article/view/12887. Acesso em: 22 jun. 2026.