Degenerative neuromuscular diseases: crucial gene and cell machinery discoveries

Lancet Neurol. 2016 Jan;15(1):12-3. doi: 10.1016/S1474-4422(15)00361-0. Epub 2015 Dec 8.

Authors

Adriano Chiò¹, Giuseppe Lauria²

Affiliations

¹ "Rita Levi Montalcini" Department of Neuroscience, University of Turin, Rome, Italy; Neuroscience Institute of Turin, Consiglio Nazionale delle Ricerche, Rome, Italy; Institute of Cognitive Sciences and Technologies, Consiglio Nazionale delle Ricerche, Rome, Italy. Electronic address: adriano.chio@unito.it.
² Department of Clinical Neurosciences, IRCCS Foundation, "Carlo Besta" Neurological Institute, Milan, Italy.

PMID: 26700898
DOI: 10.1016/S1474-4422(15)00361-0

No abstract available

Publication types

Review

MeSH terms

Amyotrophic Lateral Sclerosis / diagnosis
Amyotrophic Lateral Sclerosis / genetics
Animals
Cells / pathology
Charcot-Marie-Tooth Disease / diagnosis
Charcot-Marie-Tooth Disease / genetics
Frontotemporal Dementia / diagnosis
Frontotemporal Dementia / genetics
Humans
Myelin P0 Protein / genetics
Neuromuscular Diseases / diagnosis*
Neuromuscular Diseases / genetics*
Neuromuscular Junction / pathology

Substances

MPZ protein, human
Myelin P0 Protein