| 000 | 01800 a2200577 4500 | ||
|---|---|---|---|
| 005 | 20250515081311.0 | ||
| 264 | 0 | _c20070928 | |
| 008 | 200709s 0 0 eng d | ||
| 022 | _a1526-632X | ||
| 024 | 7 |
_a10.1212/01.wnl.0000267843.10977.4a _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aMcFarland, R | |
| 245 | 0 | 0 |
_aHomoplasmy, heteroplasmy, and mitochondrial dystonia. _h[electronic resource] |
| 260 |
_bNeurology _cAug 2007 |
||
| 300 |
_a911-6 p. _bdigital |
||
| 500 | _aPublication Type: Case Reports; Journal Article | ||
| 650 | 0 | 4 | _aAdult |
| 650 | 0 | 4 |
_aBasal Ganglia _xpathology |
| 650 | 0 | 4 |
_aBasal Ganglia Diseases _xgenetics |
| 650 | 0 | 4 | _aDNA Mutational Analysis |
| 650 | 0 | 4 |
_aDNA, Mitochondrial _xgenetics |
| 650 | 0 | 4 | _aDiagnosis, Differential |
| 650 | 0 | 4 |
_aDystonia _xgenetics |
| 650 | 0 | 4 |
_aEpilepsy _xgenetics |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 |
_aGenetic Predisposition to Disease _xgenetics |
| 650 | 0 | 4 | _aGenetic Testing |
| 650 | 0 | 4 | _aGenotype |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 |
_aInheritance Patterns _xgenetics |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aMiddle Aged |
| 650 | 0 | 4 |
_aMitochondrial Diseases _xdiagnosis |
| 650 | 0 | 4 |
_aMuscle, Skeletal _xmetabolism |
| 650 | 0 | 4 |
_aMutation _xgenetics |
| 650 | 0 | 4 |
_aOptic Atrophy, Hereditary, Leber _xgenetics |
| 650 | 0 | 4 | _aPedigree |
| 650 | 0 | 4 |
_aRNA, Transfer _xgenetics |
| 700 | 1 | _aChinnery, P F | |
| 700 | 1 | _aBlakely, E L | |
| 700 | 1 | _aSchaefer, A M | |
| 700 | 1 | _aMorris, A A M | |
| 700 | 1 | _aFoster, S M | |
| 700 | 1 | _aTuppen, H A L | |
| 700 | 1 | _aRamesh, V | |
| 700 | 1 | _aDorman, P J | |
| 700 | 1 | _aTurnbull, D M | |
| 700 | 1 | _aTaylor, R W | |
| 773 | 0 |
_tNeurology _gvol. 69 _gno. 9 _gp. 911-6 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1212/01.wnl.0000267843.10977.4a _zAvailable from publisher's website |
| 999 |
_c17254313 _d17254313 |
||