Mottled Mice and Non-Mammalian Models of Menkes Disease

Menkes disease is a multi-systemic copper metabolism disorder caused by mutations in the X-linked ATP7A gene and characterized by progressive neurodegeneration and severe connective tissue defects. The ATP7A protein is a copper (Cu)-transporting ATPase expressed in all tissues and plays a critical r...

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Detalles Bibliográficos
Autores principales: Lenartowicz, Małgorzata, Krzeptowski, Wojciech, Lipiński, Paweł, Grzmil, Paweł, Starzyński, Rafał, Pierzchała, Olga, Møller, Lisbeth Birk
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Neuroscience
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4684000/
https://www.ncbi.nlm.nih.gov/pubmed/26732058
http://dx.doi.org/10.3389/fnmol.2015.00072

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4684000/
https://www.ncbi.nlm.nih.gov/pubmed/26732058
http://dx.doi.org/10.3389/fnmol.2015.00072

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