Reply to: Double Trouble from
POLG1
and
CLCN1
Variants with Intrafamilial Phenotypic Heterogeneity
Mov Disord Clin Pract
.
2020 May 8;7(5):577-578.
doi: 10.1002/mdc3.12961.
eCollection 2020 Jul.
Authors
Martje G Pauly
1
2
,
Sinem Tunc
1
2
3
,
Tobias Bäumer
2
,
Gabriele Gillessen-Kaesbach
4
,
Alexander Münchau
2
Affiliations
1
Institute of Neurogenetics University of Lübeck Lübeck Germany.
2
Institute of Systems Motor Science University of Lübeck Lübeck Germany.
3
Department of Neurology University of Lübeck Lübeck Germany.
4
Institute of Human Genetics University of Lübeck Lübeck Germany.
PMID:
32626811
PMCID:
PMC7328426
DOI:
10.1002/mdc3.12961
No abstract available
Keywords:
CLCN1; POLG; myoclonus; myotonia congenita Thomsen.