TY  - JOUR
AU  - Burgos, Daniel F
AU  - Cusso, Lorena
AU  - Sanchez-Elexpuru, Gentzane
AU  - Calle, Daniel
AU  - Perpinya, Max Bautista
AU  - Desco, Manuel
AU  - Serratosa, Jose M
AU  - Sanchez, Marina P
PY  - 2020
DO  - 10.3390/ijms21207771
UR  - http://hdl.handle.net/20.500.12105/13179
AB  - Mutations in the EPM2A and EPM2B genes, encoding laforin and malin proteins respectively, are responsible for Lafora disease, a fatal form of progressive myoclonus epilepsy with autosomal recessive inheritance. Neuroimaging studies of patients with...
LA  - eng
PB  - Multidisciplinary Digital Publishing Institute (MDPI)
KW  - Disease Models, Animal
KW  - Animals
KW  - Atrophy
KW  - Basal Ganglia
KW  - Brain
KW  - Brain Diseases
KW  - Cerebellum
KW  - Cerebral Cortex
KW  - Glucose
KW  - Hippocampus
KW  - Humans
KW  - Lafora Disease
KW  - Magnetic Resonance Imaging
KW  - Mice, Knockout
KW  - Mutation
KW  - Positron-Emission Tomography
KW  - Protein Tyrosine Phosphatases, Non-Receptor
KW  - Ubiquitin-Protein Ligases
TI  - Structural and Functional Brain Abnormalities in Mouse Models of Lafora Disease.
TY  - journal article
ER  -