TITLE

An Iranian family with congenital myasthenic syndrome caused by a novel acetylcholine receptor mutation (CHRNE K171X)

AUTHOR(S)
Soltanzadeh, P.; Müller, J. S.; Ghorbani, A.; Abicht, A.; Lochmüller, H.; Soltanzadeh, A.; Müller, J S; Lochmüller, H
PUB. DATE
July 2005
SOURCE
Journal of Neurology, Neurosurgery & Psychiatry;Jul2005, Vol. 76 Issue 7, p1039
SOURCE TYPE
Academic Journal
DOC. TYPE
case study
ABSTRACT
Presents a letter to the editor focusing on a case study of an Iranian family with congenital myasthenic syndrome caused by a novel acetylcholine receptor mutation.
ACCESSION #
17541917

 

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