000 | 01725 a2200529 4500 | ||
---|---|---|---|
005 | 20250513091444.0 | ||
264 | 0 | _c19960724 | |
008 | 199607s 0 0 eng d | ||
022 | _a0364-5134 | ||
024 | 7 |
_a10.1002/ana.410390607 _2doi |
|
040 |
_aNLM _beng _cNLM |
||
100 | 1 | _aGomez, C M | |
245 | 0 | 0 |
_aA beta-subunit mutation in the acetylcholine receptor channel gate causes severe slow-channel syndrome. _h[electronic resource] |
260 |
_bAnnals of neurology _cJun 1996 |
||
300 |
_a712-23 p. _bdigital |
||
500 | _aPublication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. | ||
650 | 0 | 4 | _aAdult |
650 | 0 | 4 | _aAlleles |
650 | 0 | 4 | _aBase Sequence |
650 | 0 | 4 | _aBinding Sites |
650 | 0 | 4 |
_aCodon _xphysiology |
650 | 0 | 4 | _aElectromyography |
650 | 0 | 4 | _aGene Amplification |
650 | 0 | 4 | _aGenome |
650 | 0 | 4 | _aHumans |
650 | 0 | 4 |
_aIon Channel Gating _xgenetics |
650 | 0 | 4 | _aMale |
650 | 0 | 4 | _aMolecular Sequence Data |
650 | 0 | 4 |
_aMuscle Fibers, Skeletal _xultrastructure |
650 | 0 | 4 |
_aMyasthenia Gravis _xdiagnosis |
650 | 0 | 4 | _aPoint Mutation |
650 | 0 | 4 | _aPolymerase Chain Reaction |
650 | 0 | 4 |
_aPolymorphism, Genetic _xgenetics |
650 | 0 | 4 |
_aReceptors, Cholinergic _xgenetics |
650 | 0 | 4 |
_aSynaptic Membranes _xgenetics |
650 | 0 | 4 | _aSyndrome |
700 | 1 | _aMaselli, R | |
700 | 1 | _aGammack, J | |
700 | 1 | _aLasalde, J | |
700 | 1 | _aTamamizu, S | |
700 | 1 | _aCornblath, D R | |
700 | 1 | _aLehar, M | |
700 | 1 | _aMcNamee, M | |
700 | 1 | _aKuncl, R W | |
773 | 0 |
_tAnnals of neurology _gvol. 39 _gno. 6 _gp. 712-23 |
|
856 | 4 | 0 |
_uhttps://doi.org/10.1002/ana.410390607 _zAvailable from publisher's website |
999 |
_c8650679 _d8650679 |