DOI:
10.1055/s-00000041
Neuropediatrics
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References
Yamashita T, Mitsui J, Shimozawa N. et al.
Ataxic form of autosomal recessive PEX10-related peroxisome biogenesis disorders with a novel compound heterozygous gene mutation and characteristic clinical phenotype.
J Neurol Sci 2017;
375 (375) 424-429
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