Batten Disease
Author:
Affiliation:
1. Department of Pediatrics, Georgia Regents University, Augusta, GA, USA
2. Department of Pediatrics, University of South Dakota, Sioux Falls, SD, USA
3. Department of Neurology, University of Rochester, Rochester, NY, USA
Abstract
Publisher
SAGE Publications
Subject
Clinical Neurology,Pediatrics, Perinatology, and Child Health
Link
http://journals.sagepub.com/doi/pdf/10.1177/0883073813493665
Reference5 articles.
1. Strikingly Different Clinicopathological Phenotypes Determined by Progranulin-Mutation Dosage
2. Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions
3. Cln3 Deltaex7/8 knock-in mice with the common JNCL mutation exhibit progressive neurologic disease that begins before birth
4. CLN3 Defines a Novel Antiapoptotic Pathway Operative in Neurodegeneration and Mediated by Ceramide
5. Update of the mutation spectrum and clinical correlations of over 360 mutations in eight genes that underlie the neuronal ceroid lipofuscinoses
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