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Clinical and biochemical spectrum of mitochondrial complex III deficiency caused by mutations in the BCS1L gene

Authors


Maria A Ramos-Arroyo
Department of Medical Genetics
Hospital Virgen del Camino
Servicio Navarro de Salud
31008 Pamplona
Spain
Tel.: 34-848-429990
Fax: 34-848-429924
e-mail: ma.ramos.arroyo@cfnavarra.es

No abstract is available for this article.

Ancillary