DOI: 10.1055/s-00029030

Journal of Pediatric Neurology

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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