Cite
HARVARD Citation
Synofzik, M. et al. (2018). De novo ITPR1 variants are a recurrent cause of early-onset ataxia, acting via loss of channel function. European journal of human genetics. pp. 1623-1634. [Online].
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Synofzik, M. et al. (2018). De novo ITPR1 variants are a recurrent cause of early-onset ataxia, acting via loss of channel function. European journal of human genetics. pp. 1623-1634. [Online].