| 000 | 01458 a2200493 4500 | ||
|---|---|---|---|
| 005 | 20250514114247.0 | ||
| 264 | 0 | _c20031201 | |
| 008 | 200312s 0 0 fre d | ||
| 022 | _a0035-3787 | ||
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aLesca, G | |
| 245 | 0 | 0 |
_a[Symptomatic carriers of dystrophinopathy with chromosome X inactivation bias]. _h[electronic resource] |
| 260 |
_bRevue neurologique _cSep 2003 |
||
| 300 |
_a775-80 p. _bdigital |
||
| 500 | _aPublication Type: Case Reports; English Abstract; Journal Article | ||
| 650 | 0 | 4 | _aAdolescent |
| 650 | 0 | 4 | _aAdult |
| 650 | 0 | 4 |
_aChromosomes, Human, X _xgenetics |
| 650 | 0 | 4 |
_aCodon, Terminator _xgenetics |
| 650 | 0 | 4 |
_aDystrophin _xgenetics |
| 650 | 0 | 4 | _aExons |
| 650 | 0 | 4 | _aFamily |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aGene Silencing |
| 650 | 0 | 4 | _aHeterozygote |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aImmunohistochemistry |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aMiddle Aged |
| 650 | 0 | 4 |
_aMuscle Weakness _xetiology |
| 650 | 0 | 4 |
_aMuscle, Skeletal _xpathology |
| 650 | 0 | 4 |
_aMuscular Dystrophies _xgenetics |
| 650 | 0 | 4 |
_aMuscular Dystrophy, Duchenne _xgenetics |
| 650 | 0 | 4 | _aPedigree |
| 700 | 1 | _aDemarquay, G | |
| 700 | 1 | _aLlense, S | |
| 700 | 1 | _aStreichenberger, N | |
| 700 | 1 | _aPetiot, P | |
| 700 | 1 | _aMichel-Calemard, L | |
| 700 | 1 | _aRécan, D | |
| 700 | 1 | _aVial, C | |
| 700 | 1 | _aOllagnon-Roman, E | |
| 773 | 0 |
_tRevue neurologique _gvol. 159 _gno. 8-9 _gp. 775-80 |
|
| 999 |
_c13446620 _d13446620 |
||