DOI:
10.1055/s-00029030
Journal of Pediatric Neurology
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References
Gerards M, Kamps R, van Oevelen J. , et al.
Exome sequencing reveals a novel Moroccan founder mutation in SLC19A3 as a new cause of early-childhood fatal Leigh syndrome.
Brain 2013;
136 (Pt 3): 882-890
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