| 000 | 01791 a2200589 4500 | ||
|---|---|---|---|
| 005 | 20250513145611.0 | ||
| 264 | 0 | _c19980804 | |
| 008 | 199808s 0 0 eng d | ||
| 022 | _a0077-8923 | ||
| 024 | 7 |
_a10.1111/j.1749-6632.1998.tb10922.x _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aMiddleton, L T | |
| 245 | 0 | 0 |
_aCongenital myasthenic syndrome. (CMS) type Ia. Clinical and genetic diversity. _h[electronic resource] |
| 260 |
_bAnnals of the New York Academy of Sciences _cMay 1998 |
||
| 300 |
_a157-66 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 | _aAdolescent |
| 650 | 0 | 4 | _aAdult |
| 650 | 0 | 4 | _aChild |
| 650 | 0 | 4 | _aChild, Preschool |
| 650 | 0 | 4 | _aChromosome Mapping |
| 650 | 0 | 4 | _aChromosomes, Human, Pair 17 |
| 650 | 0 | 4 | _aElectrodiagnosis |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aGenes, Dominant |
| 650 | 0 | 4 | _aGenes, Recessive |
| 650 | 0 | 4 | _aGenetic Linkage |
| 650 | 0 | 4 | _aGenetic Variation |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aLod Score |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aMicrosatellite Repeats |
| 650 | 0 | 4 | _aMiddle Aged |
| 650 | 0 | 4 |
_aMyasthenia Gravis _xcongenital |
| 650 | 0 | 4 | _aPedigree |
| 650 | 0 | 4 |
_aReceptors, Cholinergic _xdeficiency |
| 650 | 0 | 4 | _aSyndrome |
| 700 | 1 | _aChristodoulou, K | |
| 700 | 1 | _aDeymeer, F | |
| 700 | 1 | _aSerdaroglu, P | |
| 700 | 1 | _aOzdemir, C | |
| 700 | 1 | _aal-Qudah, A K | |
| 700 | 1 | _aal-Shehab, A | |
| 700 | 1 | _aMavromatis, I | |
| 700 | 1 | _aMylonas, I | |
| 700 | 1 | _aEvoli, A | |
| 700 | 1 | _aTsingis, M | |
| 700 | 1 | _aZamba, E | |
| 700 | 1 | _aKyriallis, K | |
| 773 | 0 |
_tAnnals of the New York Academy of Sciences _gvol. 841 _gp. 157-66 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1111/j.1749-6632.1998.tb10922.x _zAvailable from publisher's website |
| 999 |
_c9634204 _d9634204 |
||