A novel recurrent mitochondrial DNA mutation in ND3 gene is associated with isolated complex I deficiency causing Leigh syndrome and dystonia (Q79412625)
scientific article published on 01 January 2007
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Current Data About A novel recurrent mitochondrial DNA mutation in ND3 gene is associated with isolated complex I deficiency causing Leigh syndrome and dystonia
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(P577) Monday, January 1, 2007
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(P1476) "A novel recurrent mitochondrial DNA mutation in ND3 gene is associated with isolated complex I deficiency causing Leigh syndrome and dystonia" (language: en)
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(P2093) Emmanuelle Sarzi
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Michael D Brown
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Sophie Lebon
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Dominique Chretien
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Arnold Munnich
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other details
description scientific article published on 01 January 2007

External Links
(P356) 10.1002/AJMG.A.31565
(P698) 17152068