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Evidence for Phosphorylation of CLN3 Protein Associated with Batten Disease

โœ Scribed by Martin P. Michalewski; Wojciech Kaczmarski; Adam A. Golabek; Elizabeth Kida; Aleksandra Kaczmarski; Krystyna E. Wisniewski

Book ID
115582593
Publisher
Elsevier Science
Year
1998
Tongue
English
Weight
136 KB
Volume
253
Category
Article
ISSN
0006-291X

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## Abstract Batten disease, an inherited neurodegenerative storage disease affecting children, results from the autosomal recessive inheritance of mutations in __Cln3__. The function of the CLN3 protein remains unknown. A key to understanding the pathology of this devastating disease will be to elu