Tracking sex-dependent differences in a mouse model of CLN6-Batten disease

Tracking sex-dependent differences in a mouse model of CLN6-Batten disease

Abstract Background CLN6-Batten disease is a rare neurodevelopmental disorder characterized pathologically by the accumulation of lysosomal storage material, glial activation and neurodegeneration, and phenotypically by loss of vision, motor coordination, and cognitive ability, with premature death...

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Bibliographic Details
Main Authors: McKayla J. Poppens, Jacob T. Cain, Tyler B. Johnson, Katherine A. White, Samantha S. Davis, Rachel Laufmann, Alexander D. Kloth, Jill M. Weimer
Format: Article
Language:English
Published: BMC 2019-01-01
Series:Orphanet Journal of Rare Diseases
Subjects:
Neuronal ceroid lipofuscinoses
Rare disease
Lysosomal storage disorder
Neurodegenerative disease
Pediatric disease
Online Access:http://link.springer.com/article/10.1186/s13023-019-0994-8

Internet

http://link.springer.com/article/10.1186/s13023-019-0994-8

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