ArticleBMC neurology2010
POLG1 p.R722H mutation associated with multiple mtDNA deletions and a neurological phenotype.
Tuomas Komulainen et al.PubMed ↗Full text ↗Publisher ↗
No numbers read from the abstract.
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ArticleBMC neurology2010
Tuomas Komulainen et al.PubMed ↗Full text ↗Publisher ↗
No numbers read from the abstract.