Disruption in the autophagic process underlies the sensory neuropathy in dystonia musculorum mice

A homozygous mutation in the DST (dystonin) gene causes a newly identified lethal form of hereditary sensory and autonomic neuropathy in humans (HSAN-VI). DST loss of function similarly leads to sensory neuron degeneration and severe ataxia in dystonia musculorum (Dst(dt)) mice. DST is involved in m...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:Autophagy
Egile Nagusiak: Ferrier, Andrew, De Repentigny, Yves, Lynch-Godrei, Anisha, Gibeault, Sabrina, Eid, Walaa, Kuo, Daniel, Zha, Xiaohui, Kothary, Rashmi
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Taylor & Francis 2015
Gaiak:
Basic Research Paper
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC4590603/
https://ncbi.nlm.nih.gov/pubmed/26043942
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1080/15548627.2015.1052207
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