. . . . . "TPP1" . . . . "Autosomal recessive spinocerebellar ataxia 7 (SCAR7) is caused by variants in TPP1, the gene involved in classic late-infantile neuronal ceroid lipofuscinosis 2 disease (CLN2 disease)." . . . . "2018-04-05T10:17:11.353+02:00"^^ . . . . . .