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PEX10-related autosomal recessive cerebellar ataxia with hearing loss

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Correspondence to Gül Demet Kaya Özçora.

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Parents provided informed consent prior to use their child’s history information, genetic test results, photographs and video images. Signed consent form for publication was obtained.

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Kaya Özçora, G.D., Miyatake, S., Matsumoto, N. et al. PEX10-related autosomal recessive cerebellar ataxia with hearing loss. Acta Neurol Belg 120, 429–432 (2020). https://doi.org/10.1007/s13760-018-0987-8

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  • DOI: https://doi.org/10.1007/s13760-018-0987-8

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