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

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 occurrin...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:Orphanet J Rare Dis
Prif Awduron: Poppens, McKayla J., Cain, Jacob T., Johnson, Tyler B., White, Katherine A., Davis, Samantha S., Laufmann, Rachel, Kloth, Alexander D., Weimer, Jill M.
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: BioMed Central 2019
Pynciau:
Research
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC6341540/
https://ncbi.nlm.nih.gov/pubmed/30665444
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13023-019-0994-8
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