| 000 | 01510 a2200469 4500 | ||
|---|---|---|---|
| 005 | 20250513155129.0 | ||
| 264 | 0 | _c19990204 | |
| 008 | 199902s 0 0 eng d | ||
| 022 | _a0960-8966 | ||
| 024 | 7 |
_a10.1016/s0960-8966(98)00065-0 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aNaom, I | |
| 245 | 0 | 0 |
_aLaminin alpha 2-chain gene mutations in two siblings presenting with limb-girdle muscular dystrophy. _h[electronic resource] |
| 260 |
_bNeuromuscular disorders : NMD _cOct 1998 |
||
| 300 |
_a495-501 p. _bdigital |
||
| 500 | _aPublication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 | _aBase Sequence |
| 650 | 0 | 4 | _aBiopsy |
| 650 | 0 | 4 |
_aBrain _xdiagnostic imaging |
| 650 | 0 | 4 | _aChild |
| 650 | 0 | 4 | _aDNA Mutational Analysis |
| 650 | 0 | 4 | _aElectrophysiology |
| 650 | 0 | 4 | _aFamily Health |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 |
_aLaminin _xgenetics |
| 650 | 0 | 4 | _aMagnetic Resonance Imaging |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 |
_aMuscles _xinnervation |
| 650 | 0 | 4 |
_aMuscular Dystrophies _xdiagnosis |
| 650 | 0 | 4 | _aPedigree |
| 650 | 0 | 4 | _aPoint Mutation |
| 650 | 0 | 4 | _aRadionuclide Imaging |
| 700 | 1 | _aD'Alessandro, M | |
| 700 | 1 | _aSewry, C A | |
| 700 | 1 | _aPhilpot, J | |
| 700 | 1 | _aManzur, A Y | |
| 700 | 1 | _aDubowitz, V | |
| 700 | 1 | _aMuntoni, F | |
| 773 | 0 |
_tNeuromuscular disorders : NMD _gvol. 8 _gno. 7 _gp. 495-501 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1016/s0960-8966(98)00065-0 _zAvailable from publisher's website |
| 999 |
_c9793397 _d9793397 |
||