M. Schmiedt

Novel interactions of CLN5 support molecular networking between Neuronal Ceroid Lipofuscinosis proteins

A. Jalanko, Tessa Sipilä, C. Heine, 2009, BMC Cell Biology.

Exacerbated neuronal ceroid lipofuscinosis phenotype in Cln1/5 double-knockout mice

J. Cooper, M. Jauhiainen, J. Soronen, 2012, Disease Models & Mechanisms.

Retention of lysosomal protein CLN5 in the endoplasmic reticulum causes neuronal ceroid lipofuscinosis in Asian Sibship

F. Rüschendorf, T. Braulke, K. Saar, 2008, Human mutation.

Cln5-deficiency in mice leads to microglial activation, defective myelination and changes in lipid metabolism

E. Ikonen, J. Cooper, M. Jauhiainen, 2012, Neurobiology of Disease.

The neuronal ceroid lipofuscinosis protein CLN5: new insights into cellular maturation, transport, and consequences of mutations

A. Jalanko, C. Heine, A. Kyttälä, 2010, Human mutation.

The CLN5 disease : protein maturation, trafficking and pathology

M. Schmiedt, 2012 .

Cln5-deficiency in mice leads to microglial activation, defective myelination and changes in lipid metabolism

E. Ikonen, J. Cooper, M. Jauhiainen, 2012, Neurobiology of Disease.