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Huntington’s Disease and the Striatal Medium Spiny Neuron: Cell-Autonomous and Non-Cell-Autonomous Mechanisms of Disease

Huntington’s disease is an autosomal dominant disorder caused by a mutation in the gene encoding the protein huntingtin on chromosome 4. The mutation is an expanded CAG repeat in the first exon, encoding a polyglutamine tract. If the polyglutamine tract is >40, penetrance is 100% and death is ine...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Egile nagusia: Ehrlich, Michelle E.
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Springer-Verlag 2012
Gaiak:
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC3337013/
https://ncbi.nlm.nih.gov/pubmed/22441874
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s13311-012-0112-2
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