A mouse model for Finnish variant late infantile neuronal ceroid lipofuscinosis, CLN5, reveals neuropathology associated with early aging

O Kopra, J Vesa, C von Schantz, T Manninen, H Minye, A L Fabritius, J Rapola, O P van Diggelen, J Saarela, Anu Jalanko, Leena Palotie

Research output: Contribution to journalArticleScientificpeer-review

Original languageEnglish
JournalHuman Molecular Genetics
Volume13
Pages (from-to)2893-2906
Number of pages14
ISSN0964-6906
DOIs
Publication statusPublished - 2004
MoE publication typeA1 Journal article-refereed

Fields of Science

  • BATTEN-DISEASE
  • MND MOUSE
  • MICE
  • EXPRESSION
  • PATHOLOGY
  • PROTEIN
  • INFLAMMATION
  • DEGENERATION
  • DISRUPTION
  • ISOCORTEX

Cite this

Kopra, O., Vesa, J., von Schantz, C., Manninen, T., Minye, H., Fabritius, A. L., Rapola, J., van Diggelen, O. P., Saarela, J., Jalanko, A., & Palotie, L. (2004). A mouse model for Finnish variant late infantile neuronal ceroid lipofuscinosis, CLN5, reveals neuropathology associated with early aging. Human Molecular Genetics, 13, 2893-2906. https://doi.org/10.1093/hmg/ddh312