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HUMU.22292
HUMU.22292
http://dx.doi.org/10.1002/HUMU.22292
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).
P356
Q46145781-0E2C4573-C661-4E6C-B5A3-F599443B6FE9
P356
HUMU.22292
http://dx.doi.org/10.1002/HUMU.22292