000 01223 a2200337 4500
005 20250513145611.0
264 0 _c19980804
008 199808s 0 0 eng d
022 _a0077-8923
024 7 _a10.1111/j.1749-6632.1998.tb10929.x
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aHarper, C M
245 0 0 _aSafety and efficacy of quinidine sulfate in slow-channel congenital myasthenic syndrome.
_h[electronic resource]
260 _bAnnals of the New York Academy of Sciences
_cMay 1998
300 _a203-6 p.
_bdigital
500 _aPublication Type: Clinical Trial; Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
650 0 4 _aAdolescent
650 0 4 _aAdult
650 0 4 _aAged
650 0 4 _aChild
650 0 4 _aHumans
650 0 4 _aMiddle Aged
650 0 4 _aMyasthenia Gravis
_xdrug therapy
650 0 4 _aPoint Mutation
650 0 4 _aQuinidine
_xadverse effects
650 0 4 _aReceptors, Cholinergic
_xgenetics
650 0 4 _aSyndrome
700 1 _aEngel, A G
773 0 _tAnnals of the New York Academy of Sciences
_gvol. 841
_gp. 203-6
856 4 0 _uhttps://doi.org/10.1111/j.1749-6632.1998.tb10929.x
_zAvailable from publisher's website
999 _c9634210
_d9634210