A novel gain-of-function mutation in the ITPR1 suppressor domain causes spinocerebellar ataxia with altered Ca2+ signal patterns
Casey, Jillian P., Hirouchi, Taisei, Hisatsune, Chihiro, Lynch, Bryan, Murphy, Raymond, Dunne, Aimee M., Miyamoto, Akitoshi, Ennis, Sean, van der Spek, Nick, O’Hici, Bronagh, Mikoshiba, Katsuhiko, Lynch, Sally Ann
Published in Journal of neurology (01.07.2017)
Published in Journal of neurology (01.07.2017)
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Journal Article
Fine mapping and association studies in a candidate region for autism on chromosome 2q31-q32
Conroy, Judith, Cochrane, Lynne, Anney, Richard J.L., Sutcliffe, James S., Carthy, Paula, Dunlop, Adam, Mullarkey, Marice, O'hIci, Bronagh, Green, Andrew J., Ennis, Sean, Gill, Michael, Gallagher, Louise
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (05.06.2009)
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (05.06.2009)
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Journal Article
A novel gain-of-function mutation in the ITPR1 suppressor domain causes spinocerebellar ataxia with altered Ca^sup 2+^ signal patterns
Casey, Jillian P, Hirouchi, Taisei, Hisatsune, Chihiro, Lynch, Bryan, Murphy, Raymond, Dunne, Aimee M, Miyamoto, Akitoshi, Ennis, Sean, van der Spek, Nick, O'hici, Bronagh, Mikoshiba, Katsuhiko, Lynch, Sally Ann
Published in Journal of neurology (01.07.2017)
Published in Journal of neurology (01.07.2017)
Get full text
Journal Article
A novel gain-of-function mutation in the ITPR1 suppressor domain causes spinocerebellar ataxia with altered Ca 2+ signal patterns
Casey, Jillian P, Hirouchi, Taisei, Hisatsune, Chihiro, Lynch, Bryan, Murphy, Raymond, Dunne, Aimee M, Miyamoto, Akitoshi, Ennis, Sean, van der Spek, Nick, O'Hici, Bronagh, Mikoshiba, Katsuhiko, Lynch, Sally Ann
Published in Journal of neurology (01.07.2017)
Get full text
Published in Journal of neurology (01.07.2017)
Journal Article