L. Lonka

Localization of wild‐type and mutant neuronal ceroid lipofuscinosis CLN8 proteins in non‐neuronal and neuronal cells

T. Salonen, A. Jalanko, A. Lehesjoki, 2004, Journal of neuroscience research.

The neuronal ceroid lipofuscinosis Cln8 gene expression is developmentally regulated in mouse brain and up-regulated in the hippocampal kindling model of epilepsy

M. Saarma, A. Lehesjoki, Z. Kokaia, 2005, BMC Neuroscience.

The neuronal ceroid lipofuscinosis CLN8 membrane protein is a resident of the endoplasmic reticulum.

A. Jalanko, A. Lehesjoki, A. Kyttälä, 2000, Human molecular genetics.

Turkish variant late infantile neuronal ceroid lipofuscinosis (CLN7) may be allelic to CLN8.

A. Lehesjoki, S. Mole, W. Mitchell, 2001, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Topology and endoplasmic reticulum retention signals of the lysosomal storage disease-related membrane protein CLN6

T. Braulke, S. Storch, A. Lehesjoki, 2007, Molecular membrane biology.

Neuronal ceroid lipofuscinosis CLN8 - from gene to protein

L. Lonka, Liina Lonka, 2004 .

CLN 8-FROM GENE TO PROTEIN

L. Lonka, A. Lehesjoki, Liina Lonka, 2004 .

BMC Neuroscience BioMed Central

M. Saarma, A. Lehesjoki, Z. Kokaia, 2003 .

The neuronal ceroid lipofuscinoses in human EPMR and mnd mutant mice are associated with mutations in CLN8

A. Chapelle, T. Gilliam, M. Soares, 1999, Nature Genetics.