Associated Papers
The genotype/phenotype conundrum of inherited mitochondrial disorders: Insights from a survey of mtDNA mutations associated with Leigh syndrome in complex I.
Ahmadi ZA et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease, 2025
Second-site suppressor mutations for the Asp-66-->Cys mutant of the transposon Tn10-encoded metal-tetracycline/H+ antiporter of Escherichia coli.
Yamaguchi A et al.
Biochemistry, 1995
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