DOI: 10.1055/s-00029030

Journal of Pediatric Neurology

References

Zeng WQ, Al-Yamani E, Acierno Jr JS. , et al.
Biotin-responsive basal ganglia disease maps to 2q36.3 and is due to mutations in SLC19A3.

Am J Hum Genet 2005;
77 (01) 16-26

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