Cite
HARVARD Citation
Schöggl, J. et al. (2022). A De Novo Missense NPTX1 Variant in an Individual with Infantile‐Onset Cerebellar Ataxia. Movement disorders. 37 (8), pp. 1774-1776. [Online].
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Schöggl, J. et al. (2022). A De Novo Missense NPTX1 Variant in an Individual with Infantile‐Onset Cerebellar Ataxia. Movement disorders. 37 (8), pp. 1774-1776. [Online].