Spinocerebellar ataxia type 13 mutation that is associated with disease onset in infancy disrupts axonal pathfinding during neuronal development

by Fadi A. Issa, Allan F. Mock, Alvaro Sagasti, Diane M. Papazian
Published 2012-11-01

Rapid development of Purkinje cell excitability, functional cerebellar circuit, and afferent sensory input to cerebellum in zebrafish

by Jui-Yi eHsieh, Brittany eUlrich, Fadi A. Issa, Jijun eWan, Diane M. Papazian
Published 2014-12-01

Infant and adult SCA13 mutations differentially affect Purkinje cell excitability, maturation, and viability in vivo

by Jui-Yi Hsieh, Brittany N Ulrich, Fadi A Issa, Meng-chin A Lin, Brandon Brown, Diane M Papazian
Published 2020-07-01

Frequency of KCNC3 DNA variants as causes of spinocerebellar ataxia 13 (SCA13).

by Karla P Figueroa, Michael F Waters, Vartan Garibyan, Thomas D Bird, Christopher M Gomez, Laura P W Ranum, Natali A Minassian, Diane M Papazian, Stefan M Pulst
Published 2011-03-01