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Reply to: Double Trouble from POLG1 and CLCN1 Variants with Intrafamilial Phenotypic Heterogeneity

Movement Disorders Clinical Practice
DOI: 10.1002/mdc3.12961
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Pauly, M. G., Tunc, S., Bäumer, T., Gillessen-Kaesbach, G., & Münchau, A. (2020, July 1). Reply to: Double Trouble from POLG1 and CLCN1 Variants with Intrafamilial Phenotypic Heterogeneity. Movement Disorders Clinical Practice. Wiley-Blackwell. https://doi.org/10.1002/mdc3.12961

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