Authors:
Triepels, RH
Hanson, BJ
van den Heuvel, LP
Sundell, L
Marusich, MF
Smeitink, JA
Capaldi, RA
Citation: Rh. Triepels et al., Human complex I defects can be resolved by monoclonal antibody analysis into distinct subunit assembly patterns, J BIOL CHEM, 276(12), 2001, pp. 8892-8897
Authors:
Loeffen, JLCM
Smeitink, JAM
Trijbels, JMF
Janssen, AJM
Triepels, RH
Sengers, RCA
van den Heuvel, LP
Citation: Jlcm. Loeffen et al., Isolated complex I deficiency in children: Clinical, biochemical and genetic aspects, HUM MUTAT, 15(2), 2000, pp. 123-134
Authors:
Triepels, RH
van den Heuvel, LP
Loeffen, JLCM
Buskens, CAF
Smeets, RJP
Gozalbo, MER
Budde, SMS
Mariman, EC
Wijburg, FA
Barth, PG
Trijbels, JMF
Smeitink, JAM
Citation: Rh. Triepels et al., Leigh syndrome associated with a mutation in the NDUFS7 (PSST) nuclear encoded subunit of complex I, ANN NEUROL, 45(6), 1999, pp. 787-790
Authors:
Loeffen, JLCM
Triepels, RH
van den Heuvel, LP
Schuelke, M
Buskens, CAF
Smeets, RJP
Trijbels, JMF
Smeitink, JAM
Citation: Jlcm. Loeffen et al., cDNA of eight nuclear encoded subunits of NADH : ubiquinone oxidoreductase: Human complex I cDNA characterization completed, BIOC BIOP R, 253(2), 1998, pp. 415-422