| 000 | 01055 a2200301 4500 | ||
|---|---|---|---|
| 005 | 20250515074238.0 | ||
| 264 | 0 | _c20071011 | |
| 008 | 200710s 0 0 eng d | ||
| 022 | _a1750-1172 | ||
| 024 | 7 |
_a10.1186/1750-1172-2-31 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aJungbluth, Heinz | |
| 245 | 0 | 0 |
_aMulti-minicore Disease. _h[electronic resource] |
| 260 |
_bOrphanet journal of rare diseases _cJul 2007 |
||
| 300 |
_a31 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Review | ||
| 650 | 0 | 4 | _aGenetic Heterogeneity |
| 650 | 0 | 4 | _aGenetic Predisposition to Disease |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 |
_aMuscle Proteins _xgenetics |
| 650 | 0 | 4 | _aMutation |
| 650 | 0 | 4 |
_aMyopathy, Central Core _xgenetics |
| 650 | 0 | 4 |
_aNeuromuscular Diseases _xgenetics |
| 650 | 0 | 4 |
_aRyanodine Receptor Calcium Release Channel _xgenetics |
| 650 | 0 | 4 |
_aSelenoproteins _xgenetics |
| 773 | 0 |
_tOrphanet journal of rare diseases _gvol. 2 _gp. 31 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1186/1750-1172-2-31 _zAvailable from publisher's website |
| 999 |
_c17165900 _d17165900 |
||