Ralf Triepels

The First Nuclear-Encoded Complex I Mutation in a Patient with Leigh Syndrome

Jan Loeffen, Ralf Triepels, Roel Smeets et al. · The American Journal of Human Genetics · 1998 · 282 citations · Full text

Mendelian Disorder, Genetic Disorder, Genetics +8

Leigh syndrome associated with a mutation in the NDUFS7 (PSST) nuclear encoded subunit of complex I

Ralf Triepels, Lambertus P. van den Heuvel, Jan Loeffen et al. · Annals of Neurology · 1999 · 192 citations · Full text

Impaired complex I assembly in a Leigh syndrome patient with a novel missense mutation in the ND6 gene

Cristina Ugalde, Ralf Triepels, Marieke J. H. Coenen et al. · Annals of Neurology · 2003 · 113 citations

cDNA of Eight Nuclear Encoded Subunits of NADH:Ubiquinone Oxidoreductase: Human Complex I cDNA Characterization Completed

Jan Loeffen, Ralf Triepels, Lambertus P. van den Heuvel et al. · Biochemical and Biophysical Research Communications · 1998 · 86 citations

Human Complex, Aldo-keto Reductase, Aldehyde Dehydrogenase +6

Human Complex I Defects Can Be Resolved by Monoclonal Antibody Analysis into Distinct Subunit Assembly Patterns

Ralf Triepels, Bonnie J. Hanson, Lambert P. van den Heuvel et al. · Journal of Biological Chemistry · 2001 · 60 citations · Full text