DOI:
10.1055/s-00029027
Journal of Pediatric Genetics
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References
Reihle C, von Kalle T, Severien C. , et al.
Biotin-responsive basal ganglia disease in a 10- year-old German girl without SLC19A3 gene mutation.
Neuropediatrics 2013;44. doi: 10.1055/s-0033-1337842
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