High intra-familiar clinical variability in MORC2 mutated CMT2 patients
Brain
.
2017 Apr 1;140(4):e21.
doi: 10.1093/brain/awx019.
Authors
Claudio Semplicini
1
2
,
Elisabeth Ollagnon-Roman
3
,
Sarah Leonard-Louis
1
,
Guenaelle Piguet-Lacroix
4
,
Manon Silvestre
4
,
Philippe Latour
4
,
Tanya Stojkovic
1
Affiliations
1
G-H Pitié-Salpêtrière, Institut de Myologie, centre de référence des maladies neuromusculaires Paris Est, France.
2
Department of Neuroscience, University of Padova, Padova, Italy.
3
Service de Neurogénétique, Hôpital de la Croix-Rousse, Hospices Civils de Lyon, Lyon, France.
4
Service de Neurobiologie, Centre de Biologie Est, Hospices Civils de Lyon, Lyon, France.
PMID:
28334961
DOI:
10.1093/brain/awx019
No abstract available
Publication types
Letter
Comment
MeSH terms
Axons
Charcot-Marie-Tooth Disease*
Humans
Mutation*
Transcription Factors / genetics
Substances
MORC2 protein, human
Transcription Factors