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Erratum to: The frequency of spinocerebellar ataxia type 23 in a UK population

✍ Scribed by Katherine Fawcett, Mohadeseh Mehrabian, Yo-Tsen Liu, Sherifa Hamed…


Book ID
120898473
Publisher
Springer
Year
2012
Tongue
English
Weight
111 KB
Volume
260
Category
Article
ISSN
0340-5354

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## Abstract Spinocerebellar ataxia type 14 (SCA14) is an autosomal dominant neurodegenerative disorder characterized by cerebellar ataxia and intermittent axial myoclonus. Various mutations have been found in the PRKCG gene encoding protein kinase C γ in SCA14 families. Most of those mutations have