Marked phenotypic variability in two siblings with congenital myasthenic syndrome due to mutations in MUSK
J Neurol
.
2013 Oct 12:10.1007/s00415-013-7118-5.
doi: 10.1007/s00415-013-7118-5.
Online ahead of print.
Authors
Lorenzo Maggi
1
,
R Brugnoni
,
V Scaioli
,
T L Winden
,
L Morandi
,
A G Engel
,
R Mantegazza
,
P Bernasconi
Affiliation
1
Neuroimmunology and Neuromuscular Diseases Unit, Foundation IRCCS Neurological Institute "Carlo Besta", Via Celoria 11, 20133, Milan, Italy, lorenzo.maggi@istituto-besta.it.
PMID:
24122059
PMCID:
PMC3984612
DOI:
10.1007/s00415-013-7118-5
No abstract available
Grants and funding
R01 NS006277/NS/NINDS NIH HHS/United States