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...

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Detalhes bibliográficos
Publicado no:Orphanet J Rare Dis
Main Authors: Poppens, McKayla J., Cain, Jacob T., Johnson, Tyler B., White, Katherine A., Davis, Samantha S., Laufmann, Rachel, Kloth, Alexander D., Weimer, Jill M.
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2019
Assuntos:
Research
Acesso em linha: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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