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Simone Olgiati MSc,
Simone Olgiati MSc
Department of Clinical Genetics, Erasmus MC, Rotterdam, the Netherlands
Search for more papers by this author Marialuisa Quadri PhD,
Marialuisa Quadri PhD
Department of Clinical Genetics, Erasmus MC, Rotterdam, the Netherlands
Search for more papers by this author Wim Mandemakers PhD,
Wim Mandemakers PhD
Department of Clinical Genetics, Erasmus MC, Rotterdam, the Netherlands
Search for more papers by this author Vincenzo Bonifati MD, PhD,
Vincenzo Bonifati MD, PhD
Department of Clinical Genetics, Erasmus MC, Rotterdam, the Netherlands
Search for more papers by this author
Simone Olgiati MSc,
Simone Olgiati MSc
Department of Clinical Genetics, Erasmus MC, Rotterdam, the Netherlands
Search for more papers by this author Marialuisa Quadri PhD,
Marialuisa Quadri PhD
Department of Clinical Genetics, Erasmus MC, Rotterdam, the Netherlands
Search for more papers by this author Wim Mandemakers PhD,
Wim Mandemakers PhD
Department of Clinical Genetics, Erasmus MC, Rotterdam, the Netherlands
Search for more papers by this author Vincenzo Bonifati MD, PhD,
Vincenzo Bonifati MD, PhD
Department of Clinical Genetics, Erasmus MC, Rotterdam, the Netherlands
Search for more papers by this author
First published: 24 December 2015
No abstract is available for this article.
References
- 1Olgiati S, Quadri M, Fang M, et al. DNAJC6 mutations associated with early onset Parkinson disease. Ann Neurol 2016; DOI: 10.1002/ana.24553
- 2Edvardson S, Cinnamon Y, Ta-Shma A, et al. A deleterious mutation in DNAJC6 encoding the neuronal-specific clathrin-uncoating co-chaperone auxilin, is associated with juvenile parkinsonism. PLoS One 2012; 7: e36458.
- 3Koroglu C, Baysal L, Cetinkaya M, et al. DNAJC6 is responsible for juvenile parkinsonism with phenotypic variability. Parkinsonism Relat Disord 2013; 19: 320–324.
