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HARVARD Citation
Nissenkorn, A. et al. (n.d.). Mutations in AIFM1 cause a potentially treatable X-linked childhood cerebellar ataxia. European journal of paediatric neurology. pp. e214-. [Online].
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Nissenkorn, A. et al. (n.d.). Mutations in AIFM1 cause a potentially treatable X-linked childhood cerebellar ataxia. European journal of paediatric neurology. pp. e214-. [Online].