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Petry-Schmelzer, J. et al. (2021). P 27. VPS13D: One family, one mutation, two phenotypes. Clinical neurophysiology. 132 (8), pp. e12-e13. [Online].
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Petry-Schmelzer, J. et al. (2021). P 27. VPS13D: One family, one mutation, two phenotypes. Clinical neurophysiology. 132 (8), pp. e12-e13. [Online].