| 000 | 01120 a2200325 4500 | ||
|---|---|---|---|
| 005 | 20250517223756.0 | ||
| 264 | 0 | _c20191023 | |
| 008 | 201910s 0 0 eng d | ||
| 022 | _a1873-2364 | ||
| 024 | 7 |
_a10.1016/j.nmd.2018.05.006 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aFindlay, Andrew R | |
| 245 | 0 | 0 |
_aHomozygous recessive MYH2 mutation mimicking dominant MYH2 associated myopathy. _h[electronic resource] |
| 260 |
_bNeuromuscular disorders : NMD _c08 2018 |
||
| 300 |
_a675-679 p. _bdigital |
||
| 500 | _aPublication Type: Case Reports; Journal Article | ||
| 650 | 0 | 4 | _aAdult |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 |
_aMuscle Weakness _xgenetics |
| 650 | 0 | 4 |
_aMuscle, Skeletal _xpathology |
| 650 | 0 | 4 |
_aMuscular Diseases _xgenetics |
| 650 | 0 | 4 | _aMutation, Missense |
| 650 | 0 | 4 |
_aMyosin Heavy Chains _xgenetics |
| 700 | 1 | _aHarms, Matthew B | |
| 700 | 1 | _aPestronk, Alan | |
| 700 | 1 | _aWeihl, Conrad C | |
| 773 | 0 |
_tNeuromuscular disorders : NMD _gvol. 28 _gno. 8 _gp. 675-679 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1016/j.nmd.2018.05.006 _zAvailable from publisher's website |
| 999 |
_c28561202 _d28561202 |
||