Molecular Mechanisms and Therapeutics for Spinocerebellar Ataxia Type 2
Author:
Funder
NINDS
Publisher
Springer Science and Business Media LLC
Subject
Pharmacology (medical),Clinical Neurology,Pharmacology
Link
http://link.springer.com/content/pdf/10.1007/s13311-019-00777-6.pdf
Reference233 articles.
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2. Magana JJ, Velazquez-Perez L, Cisneros B. Spinocerebellar ataxia type 2: clinical presentation, molecular mechanisms, and therapeutic perspectives. Mol Neurobiol 2013;47(1):90–104.
3. Paulson HL, Shakkottai VG, Clark HB, Orr HT. Polyglutamine spinocerebellar ataxias—from genes to potential treatments. Nat Rev Neurosci 2017;18(10):613–26.
4. Scoles DR, Pulst SM. Spinocerebellar ataxia type 2. Adv Exp Med Biol 2018;1049:175–95.
5. Buijsen RAM, Toonen LJA, Gardiner SL, van Roon-Mom WMC. Genetics, mechanisms, and therapeutic progress in polyglutamine spinocerebellar ataxias. Neurotherapeutics. 2019.
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