VPS13D: One Family, Same Mutations, Two Phenotypes
Mov Disord Clin Pract
.
2021 May 5;8(5):803-806.
doi: 10.1002/mdc3.13232.
eCollection 2021 Jul.
Authors
Jan Niklas Petry-Schmelzer
1
,
Natalie Keller
2
3
,
Mert Karakaya
2
3
,
Brunhilde Wirth
2
3
,
Gereon R Fink
1
4
,
Gilbert Wunderlich
1
3
Affiliations
1
Faculty of Medicine and University Hospital Cologne, Department of Neurology University of Cologne Cologne Germany.
2
Faculty of Medicine and University Hospital Cologne, Institute of Human Genetics,Center of Molecular Medicine University of Cologne Cologne Germany.
3
Faculty of Medicine and University Hospital Cologne, Center for Rare Diseases University of Cologne Cologne Germany.
4
Institute of Neuroscience and Medicine (INM-3), Research Center Jülich Cognitive Neuroscience Jülich Germany.
PMID:
34307758
PMCID:
PMC8287157
DOI:
10.1002/mdc3.13232
No abstract available
Keywords:
VPS13D; phenotype–genotype correlation.