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. 2003 Dec;40(12):896–899. doi: 10.1136/jmg.40.12.896
Recurrent de novo mitochondrial DNA mutations in respiratory chain deficiency
S Lebon
1, M Chol
1, P Benit
1, C Mugnier
1, D Chretien
1, I Giurgea
1, I Kern
1, E Girardin
1, L Hertz-Pannier
1, P de Lonlay
1, A Rotig
1, P Rustin
1, A Munnich
1
S Lebon
1INSERM U393, Department of Genetics, Hôpital Necker-Enfants Malades, 149 rue de Sèvres, 75015 Paris, France.
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M Chol
1INSERM U393, Department of Genetics, Hôpital Necker-Enfants Malades, 149 rue de Sèvres, 75015 Paris, France.
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P Benit
1INSERM U393, Department of Genetics, Hôpital Necker-Enfants Malades, 149 rue de Sèvres, 75015 Paris, France.
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C Mugnier
1INSERM U393, Department of Genetics, Hôpital Necker-Enfants Malades, 149 rue de Sèvres, 75015 Paris, France.
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D Chretien
1INSERM U393, Department of Genetics, Hôpital Necker-Enfants Malades, 149 rue de Sèvres, 75015 Paris, France.
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I Giurgea
1INSERM U393, Department of Genetics, Hôpital Necker-Enfants Malades, 149 rue de Sèvres, 75015 Paris, France.
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I Kern
1INSERM U393, Department of Genetics, Hôpital Necker-Enfants Malades, 149 rue de Sèvres, 75015 Paris, France.
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E Girardin
1INSERM U393, Department of Genetics, Hôpital Necker-Enfants Malades, 149 rue de Sèvres, 75015 Paris, France.
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L Hertz-Pannier
1INSERM U393, Department of Genetics, Hôpital Necker-Enfants Malades, 149 rue de Sèvres, 75015 Paris, France.
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P de Lonlay
1INSERM U393, Department of Genetics, Hôpital Necker-Enfants Malades, 149 rue de Sèvres, 75015 Paris, France.
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A Rotig
1INSERM U393, Department of Genetics, Hôpital Necker-Enfants Malades, 149 rue de Sèvres, 75015 Paris, France.
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P Rustin
1INSERM U393, Department of Genetics, Hôpital Necker-Enfants Malades, 149 rue de Sèvres, 75015 Paris, France.
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A Munnich
1INSERM U393, Department of Genetics, Hôpital Necker-Enfants Malades, 149 rue de Sèvres, 75015 Paris, France.
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1INSERM U393, Department of Genetics, Hôpital Necker-Enfants Malades, 149 rue de Sèvres, 75015 Paris, France.
PMCID: PMC1735336 PMID: 14684687