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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Detalles Bibliográficos
Autores principales: Poppens, McKayla J., Cain, Jacob T., Johnson, Tyler B., White, Katherine A., Davis, Samantha S., Laufmann, Rachel, Kloth, Alexander D., Weimer, Jill M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6341540/
https://www.ncbi.nlm.nih.gov/pubmed/30665444
http://dx.doi.org/10.1186/s13023-019-0994-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6341540/
https://www.ncbi.nlm.nih.gov/pubmed/30665444
http://dx.doi.org/10.1186/s13023-019-0994-8

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