Associated Papers
Comprehensive analysis of coding variants highlights genetic complexity in developmental and epileptic encephalopathy.
Takata A et al.
Nature Communications, 2019
31175295 (PubMed )
Supplement: 41467_2019_10482_MOESM8_ESM.xlsx › Supplementary_Data_5
Fine mapping of 16q-linked autosomal dominant cerebellar ataxia type III in Japanese families.
Hirano R et al.
Neurogenetics, 2004
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