Widening the phenotypical spectrum of EGR2-related CMT: Unusual phenotype for R409W mutation. Issue 1 (January 2019)

Record Type:: Journal Article
Title:: Widening the phenotypical spectrum of EGR2-related CMT: Unusual phenotype for R409W mutation. Issue 1 (January 2019)
Main Title:: Widening the phenotypical spectrum of EGR2-related CMT: Unusual phenotype for R409W mutation
Authors:: Leonardi, Luca
Garibaldi, Matteo
Fionda, Laura
Vanoli, Fiammetta
Loreti, Simona
Morino, Stefania
Antonini, Giovanni
Abstract:
Is Part Of:: Clinical neurophysiology. Volume 130:Issue 1(2019:Jan.)
Journal:: Clinical neurophysiology
Issue:: Volume 130:Issue 1(2019:Jan.)
Issue Display:: Volume 130, Issue 1 (2019)
Year:: 2019
Volume:: 130
Issue:: 1
Issue Sort Value:: 2019-0130-0001-0000
Page Start:: 93
Page End:: 94
Publication Date:: 2019-01
Subjects:: EGR2 -- MPZ -- CMT phenotypes spectrum -- Nerve ultrasound
Neurophysiology -- Periodicals
Electroencephalography -- Periodicals
Electromyography -- Periodicals
Neurology -- Periodicals
612.8
Journal URLs:: http://www.sciencedirect.com/science/journal/13882457 ↗
http://www.elsevier.com/journals ↗
DOI:: 10.1016/j.clinph.2018.11.007 ↗
Languages:: English
ISSNs:: 1388-2457
Deposit Type:: Legaldeposit
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗
Physical Locations:: British Library DSC - 3286.310645
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store
Ingest File:: 9062.xml