DOI:
10.1055/s-00000041
Neuropediatrics
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References
Haack TB, Madignier F, Herzer M. , et al.
Mutation screening of 75 candidate genes in 152 complex I deficiency cases identifies pathogenic variants in 16 genes including NDUFB9.
J Med Genet 2012;
49 (02) 83-89
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