Elucidation of the Molecular Mechanism and Exploration of Novel Therapeutics for Spinocerebellar Ataxia Caused by Mutant Protein Kinase Cγ
Abstract.: Spinocerebellar ataxia (SCA) is an inherited neurodegenerative disorder that is characterized by cerebellar atrophy and progressive ataxia and is classified into 31 types by the genetic locus. Recently, missense mutations of PRKCG genes that code protein kinase Cγ (γPKC) have been identif...
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| Main Authors: | , , , , , , , |
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| Format: | Book |
| Published: |
Elsevier,
2011-01-01T00:00:00Z.
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| Online Access: | Connect to this object online. |
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