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

2009; Wiley; Volume: 75; Issue: 6 Linguagem: Inglês

10.1111/j.1399-0004.2009.01160.x

1399-0004

MA Ramos‐Arroyo, J. Barado Hualde, A. Ayechu, Linda De Meırleır, Sara Seneca, Nathalie Nadal, P. Briones,

Genetics and Neurodevelopmental Disorders

Clinical GeneticsVolume 75, Issue 6 p. 585-587 Clinical and biochemical spectrum of mitochondrial complex III deficiency caused by mutations in the BCS1L gene MA Ramos-Arroyo, Corresponding Author MA Ramos-Arroyo Department of Medical GeneticsMaria A Ramos-ArroyoDepartment of Medical GeneticsHospital Virgen del CaminoServicio Navarro de Salud31008 PamplonaSpainTel.: 34-848-429990Fax: 34-848-429924e-mail: [email protected]Search for more papers by this authorJ Hualde, J Hualde Department of Pediatrics, Hospital Virgen del Camino, Pamplona, SpainSearch for more papers by this authorA Ayechu, A Ayechu Department of Pediatrics, Hospital Virgen del Camino, Pamplona, SpainSearch for more papers by this authorL De Meirleir, L De Meirleir Department of Pediatric NeurologySearch for more papers by this authorS Seneca, S Seneca Department of Medical Genetics, Free University, Brussels, BelgiumSearch for more papers by this authorN Nadal, N Nadal Department of Pediatrics, Hospital Virgen del Camino, Pamplona, SpainSearch for more papers by this authorP Briones, P Briones Institut de Bioquimica Clinica, Servei de Bioquímica i Genética Molecular, Hospital Clinic, CSIC and CIBER de Enfermedades Raras, Barcelona, SpainSearch for more papers by this author MA Ramos-Arroyo, Corresponding Author MA Ramos-Arroyo Department of Medical GeneticsMaria A Ramos-ArroyoDepartment of Medical GeneticsHospital Virgen del CaminoServicio Navarro de Salud31008 PamplonaSpainTel.: 34-848-429990Fax: 34-848-429924e-mail: [email protected]Search for more papers by this authorJ Hualde, J Hualde Department of Pediatrics, Hospital Virgen del Camino, Pamplona, SpainSearch for more papers by this authorA Ayechu, A Ayechu Department of Pediatrics, Hospital Virgen del Camino, Pamplona, SpainSearch for more papers by this authorL De Meirleir, L De Meirleir Department of Pediatric NeurologySearch for more papers by this authorS Seneca, S Seneca Department of Medical Genetics, Free University, Brussels, BelgiumSearch for more papers by this authorN Nadal, N Nadal Department of Pediatrics, Hospital Virgen del Camino, Pamplona, SpainSearch for more papers by this authorP Briones, P Briones Institut de Bioquimica Clinica, Servei de Bioquímica i Genética Molecular, Hospital Clinic, CSIC and CIBER de Enfermedades Raras, Barcelona, SpainSearch for more papers by this author First published: 01 June 2009 https://doi.org/10.1111/j.1399-0004.2009.01160.xCitations: 30Read the full textAboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onFacebookTwitterLinkedInRedditWechat Citing Literature Volume75, Issue6June 2009Pages 585-587 RelatedInformation