Axonopathy in the Central Nervous System Is the Hallmark of Mice with a Novel Intragenic Null Mutation of Dystonin

Dystonia musculorum is a neurodegenerative disorder caused by a mutation in the dystonin gene. It has been described in mice and humans where it is called hereditary sensory autonomic neuropathy. Mutated mice show severe movement disorders and die at the age of 3–4 weeks. This study describes the di...

Descripció completa

Guardat en:
Dades bibliogràfiques
Publicat a:Genetics
Autors principals: Seehusen, Frauke, Kiel, Kirsten, Jottini, Stefano, Wohlsein, Peter, Habierski, Andre, Seibel, Katharina, Vogel, Tanja, Urlaub, Henning, Kollmar, Martin, Baumgärtner, Wolfgang, Teichmann, Ulrike
Format: Artigo
Idioma:Inglês
Publicat: Genetics Society of America 2016
Matèries:
Investigations
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC5012385/
https://ncbi.nlm.nih.gov/pubmed/27401753
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1534/genetics.116.186932
Etiquetes: Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!

Ítems similars