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Table 1 List of genes linked to NCL in humans
| Protein | Disease |
|---|---|
| PPT1/CLN1 | Infantile NCL |
| TPP1/CLN2 | Late-infantile NCL |
| CLN3 | Juvenile NCL |
| DNAJC5/CLN4 | Adult-onset NCL, Kufs disease, Parry disease |
| CLN5 | Late-infantile NCL (Finnish variant) |
| CLN6 | Variant late-infantile NCL |
| MFSD8/CLN7 | Late-infantile NCL (Turkish variant) |
| CLN8 | Northern epilepsy (epilespy, progressive with mental retardation, EPMR) |
| CTSD/CLN10 | Congenital, neonatal and late infantile NCL |
| PGRN/CLN11 | Adult-onset NCL, frontotemporal dementia in heterozygotes |
| ATP13A2/CLN12 | Juvenile-onset NCL |
| CTSF/CLN13 | Adult-onset NCL |
| KCTD7/CLN14 | Infantile NCL |
