Recurrent de novo mitochondrial DNA mutations in respiratory chain deficiency.

Lebon, S; Chol, M; Benit, P; Mugnier, C; Chretien, D; Giurgea, I; Kern, I; Girardin, E; Hertz-Pannier, L; de Lonlay, P; Rötig, A; Rustin, P; Munnich, A

Lebon, S; Chol, M; Benit, P; Mugnier, C; Chretien, D; Giurgea, I; Kern, I; Girardin, E; Hertz-Pannier, L; de Lonlay, P; Rötig, A; Rustin, P; Munnich, A.

Affiliation

Lebon S; INSERM U393, Department of Genetics, Hôpital Necker-Enfants Malades, 149 rue de Sèvres, 75015 Paris, France.

J Med Genet ; 40(12): 896-9, 2003 Dec.

Article in En | MEDLINE | ID: mdl-14684687

Subject(s)

DNA, Mitochondrial/genetics; Electron Transport Complex I/genetics; Mutation; Adolescent; Adult; Child; Child, Preschool; DNA Mutational Analysis; Female; Humans; Infant; Leigh Disease/genetics; Male

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: DNA, Mitochondrial / Electron Transport Complex I / Mutation Limits: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male Language: En Journal: J Med Genet Year: 2003 Document type: Article

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