Reply to: Double Trouble from POLG1 and CLCN1 Variants with Intrafamilial Phenotypic Heterogeneity-Reference-Cited by-同舟云学术

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

Published:2020-05-08 Issue:5 Volume:7 Page:577-578
ISSN:2330-1619
Container-title:Movement Disorders Clinical Practice
language:en
Short-container-title:Mov Disord Clin Pract

Author:

Pauly Martje G.¹²^ORCID,Tunc Sinem¹²³,Bäumer Tobias²,Gillessen‐Kaesbach Gabriele⁴,Münchau Alexander²

Affiliation:

1. Institute of NeurogeneticsUniversity of Lübeck Lübeck Germany

2. Institute of Systems Motor ScienceUniversity of Lübeck Lübeck Germany

3. Department of NeurologyUniversity of Lübeck Lübeck Germany

4. Institute of Human GeneticsUniversity of Lübeck Lübeck Germany

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mdc3.12961

Reference3 articles.

1. Double trouble from POLG1 and CLCN1 variants with intra‐familial phenotypic heterogeneity;Finsterer J.;Mov Disord Clin Pract

2. “Twitching” and Stiffness in POLG1 Mutation Carriers: Red Flag or Red Herring?

3. The antimyotonic effect of lamotrigine in non-dystrophic myotonias: a double-blind randomized study

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