| 000 | 01500 a2200469 4500 | ||
|---|---|---|---|
| 005 | 20250516102945.0 | ||
| 264 | 0 | _c20121012 | |
| 008 | 201210s 0 0 eng d | ||
| 022 | _a1526-632X | ||
| 024 | 7 |
_a10.1212/WNL.0b013e318261714a _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aStamelou, Maria | |
| 245 | 0 | 0 |
_aMyoclonus-dystonia syndrome due to tyrosine hydroxylase deficiency. _h[electronic resource] |
| 260 |
_bNeurology _cJul 2012 |
||
| 300 |
_a435-41 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 | _aAdult |
| 650 | 0 | 4 | _aDNA Mutational Analysis |
| 650 | 0 | 4 |
_aDystonic Disorders _xenzymology |
| 650 | 0 | 4 | _aElectroencephalography |
| 650 | 0 | 4 | _aElectromyography |
| 650 | 0 | 4 |
_aEvoked Potentials, Somatosensory _xgenetics |
| 650 | 0 | 4 | _aFamily Health |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aGenotype |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 |
_aMedian Nerve _xphysiopathology |
| 650 | 0 | 4 |
_aPoint Mutation _xgenetics |
| 650 | 0 | 4 |
_aReflex _xgenetics |
| 650 | 0 | 4 |
_aTyrosine 3-Monooxygenase _xdeficiency |
| 650 | 0 | 4 | _aYoung Adult |
| 700 | 1 | _aMencacci, Niccolo E | |
| 700 | 1 | _aCordivari, Carla | |
| 700 | 1 | _aBatla, Amit | |
| 700 | 1 | _aWood, Nick W | |
| 700 | 1 | _aHoulden, Henry | |
| 700 | 1 | _aHardy, John | |
| 700 | 1 | _aBhatia, Kailash P | |
| 773 | 0 |
_tNeurology _gvol. 79 _gno. 5 _gp. 435-41 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1212/WNL.0b013e318261714a _zAvailable from publisher's website |
| 999 |
_c21960966 _d21960966 |
||