A novel CLN2/TPP1 mutation in a patient with late infantile neuronal ceroid lipofuscinosis
- PMID: 26032578
- DOI: 10.1007/s10072-015-2272-4
A novel CLN2/TPP1 mutation in a patient with late infantile neuronal ceroid lipofuscinosis
Keywords: Ceroid lipofuscinosis neuronal 2; Late infantile neuronal ceroid lipofuscinoses (LINCL); Neuronal ceroid lipofuscinoses (NCL); Novel gene mutation; Tripeptidyl-peptidase 1.