A novel missense mutation in SUCLG1 associated with mitochondrial DNA depletion, encephalomyopathic form, with methylmalonic aciduria.
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A novel missense mutation in SUCLG1 associated with mitochondrial DNA depletion, encephalomyopathic form, with methylmalonic aciduria.
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External Links
| (P356) |
10.1007/S00431-009-1007-Z
|
| (P698) |
19526370
|
| (P6179) |
1048531510
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