New mutations in protein kinase Cγ associated with spinocerebellar ataxia type 14-Reference-Cited by-同舟云学术

New mutations in protein kinase Cγ associated with spinocerebellar ataxia type 14

Published:2005 Issue:5 Volume:58 Page:720-729
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Klebe Stephan,Durr Alexandra,Rentschler Alexander,Hahn-Barma Valerie,Abele Michael,Bouslam Naima,Schöls Ludger,Jedynak Pierre,Forlani Sylvie,Denis Elodie,Dussert Christel,Agid Yves,Bauer Peter,Globas Christoph,Wüllner Ullrich,Brice Alexis,Riess Olaf,Stevanin Giovanni

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Reference34 articles.

1. Autosomal dominant cerebellar ataxias: clinical features, genetics, and pathogenesis

2. Pathways to motor incoordination: the inherited ataxias

3. A novel locus for dominant cerebellar ataxia (SCA14) maps to a 10.2-cM interval flanked by D19S206 and D19S605 on chromosome 19q13.4-qter

4. A New Dominant Spinocerebellar Ataxia Linked to Chromosome 19q13.4-qter

5. Protein Kinase C: Structure, Function, and Regulation

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