APA

Bénit P., Steffann J., Lebon S., Chretien D., Kadhom N., de Lonlay P., Goldenberg A., Dumez Y., Dommergues M., Rustin P., Munnich A. & Rötig A. (20030618). Genotyping microsatellite DNA markers at putative disease loci in inbred/multiplex families with respiratory chain complex I deficiency allows rapid identification of a novel nonsense mutation (IVS1nt -1) in the NDUFS4 gene in Leigh syndrome. : Human genetics.

Chicago

Bénit Paule, Steffann Julie, Lebon Sophie, Chretien Dominique, Kadhom Noman, de Lonlay Pascale, Goldenberg Alice, Dumez Yves, Dommergues Marc, Rustin Pierre, Munnich Arnold and Rötig Agnès. 20030618. Genotyping microsatellite DNA markers at putative disease loci in inbred/multiplex families with respiratory chain complex I deficiency allows rapid identification of a novel nonsense mutation (IVS1nt -1) in the NDUFS4 gene in Leigh syndrome. : Human genetics.

Harvard

Bénit P., Steffann J., Lebon S., Chretien D., Kadhom N., de Lonlay P., Goldenberg A., Dumez Y., Dommergues M., Rustin P., Munnich A. and Rötig A. (20030618). Genotyping microsatellite DNA markers at putative disease loci in inbred/multiplex families with respiratory chain complex I deficiency allows rapid identification of a novel nonsense mutation (IVS1nt -1) in the NDUFS4 gene in Leigh syndrome. : Human genetics.

MLA

Bénit Paule, Steffann Julie, Lebon Sophie, Chretien Dominique, Kadhom Noman, de Lonlay Pascale, Goldenberg Alice, Dumez Yves, Dommergues Marc, Rustin Pierre, Munnich Arnold and Rötig Agnès. Genotyping microsatellite DNA markers at putative disease loci in inbred/multiplex families with respiratory chain complex I deficiency allows rapid identification of a novel nonsense mutation (IVS1nt -1) in the NDUFS4 gene in Leigh syndrome. : Human genetics. 20030618.