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Caglayan, A. et al. (2021). Biallelic ZNF335 mutations cause basal ganglia abnormality with progressive cerebral/cerebellar atrophy. Journal of neurogenetics. pp. 23-28. [Online].
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Caglayan, A. et al. (2021). Biallelic ZNF335 mutations cause basal ganglia abnormality with progressive cerebral/cerebellar atrophy. Journal of neurogenetics. pp. 23-28. [Online].