N. R. Whaley, S. Fujioka, Z. K. Wszolek: Autosomal dominant cerebellar ataxia type I: a review of the phenotypic and genotypic characteristics. In: Orphanet Journal of Rare Diseases. Band 6, Mai 2011, S. 33, doi:10.1186/1750-1172-6-33, PMID 21619691, PMC 3123548 (freier Volltext) (Review).
A. Catania, L. Peverelli, S. Tabano, D. Ghezzi, C. Lamperti: DNMT1-complex disorder caused by a novel mutation associated with an overlapping phenotype of autosomal-dominant cerebellar ataxia, deafness, and narcolepsy (ADCA-DN) and hereditary sensory neuropathy with dementia and hearing loss (HSN1E). In: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology. Band 40, Nummer 9, September 2019, S. 1963–1966, doi:10.1007/s10072-019-03859-7, PMID 30911858.
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N. R. Whaley, S. Fujioka, Z. K. Wszolek: Autosomal dominant cerebellar ataxia type I: a review of the phenotypic and genotypic characteristics. In: Orphanet Journal of Rare Diseases. Band 6, Mai 2011, S. 33, doi:10.1186/1750-1172-6-33, PMID 21619691, PMC 3123548 (freier Volltext) (Review).
A. Catania, L. Peverelli, S. Tabano, D. Ghezzi, C. Lamperti: DNMT1-complex disorder caused by a novel mutation associated with an overlapping phenotype of autosomal-dominant cerebellar ataxia, deafness, and narcolepsy (ADCA-DN) and hereditary sensory neuropathy with dementia and hearing loss (HSN1E). In: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology. Band 40, Nummer 9, September 2019, S. 1963–1966, doi:10.1007/s10072-019-03859-7, PMID 30911858.
