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

Martje G. Pauly, Sinem Tunc, Tobias Bäumer, Gabriele Gillessen-Kaesbach, Alexander Münchau*

*Corresponding author for this work
Original languageEnglish
JournalMovement Disorders Clinical Practice
Issue number5
Pages (from-to)577-578
Number of pages2
Publication statusPublished - 01.07.2020

Research Areas and Centers

  • Research Area: Medical Genetics

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