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Heimer, G. et al. (n.d.). Mutations in AIFM1 cause an X-linked childhood cerebellar ataxia partially responsive to riboflavin. European journal of paediatric neurology. pp. 93-101. [Online].
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Heimer, G. et al. (n.d.). Mutations in AIFM1 cause an X-linked childhood cerebellar ataxia partially responsive to riboflavin. European journal of paediatric neurology. pp. 93-101. [Online].