| 000 | 01291 a2200385 4500 | ||
|---|---|---|---|
| 005 | 20250514155533.0 | ||
| 264 | 0 | _c20031023 | |
| 008 | 200310s 0 0 eng d | ||
| 022 | _a0012-1622 | ||
| 024 | 7 |
_a10.1017/s0012162203001300 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aKeng, W T | |
| 245 | 0 | 0 |
_aA3243G mitochondrial mutation associated with polymicrogyria. _h[electronic resource] |
| 260 |
_bDevelopmental medicine and child neurology _cOct 2003 |
||
| 300 |
_a704-8 p. _bdigital |
||
| 500 | _aPublication Type: Case Reports; Journal Article | ||
| 650 | 0 | 4 | _aAdolescent |
| 650 | 0 | 4 |
_aBrain _xabnormalities |
| 650 | 0 | 4 |
_aCalcinosis _xpathology |
| 650 | 0 | 4 | _aChild |
| 650 | 0 | 4 |
_aDNA, Mitochondrial _xgenetics |
| 650 | 0 | 4 | _aDiffusion Magnetic Resonance Imaging |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 |
_aGene Expression _xgenetics |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 |
_aMELAS Syndrome _xdiagnosis |
| 650 | 0 | 4 | _aPhenotype |
| 650 | 0 | 4 |
_aPoint Mutation _xgenetics |
| 650 | 0 | 4 | _aTomography, X-Ray Computed |
| 700 | 1 | _aPilz, D T | |
| 700 | 1 | _aMinns, B | |
| 700 | 1 | _aFitzPatrick, D R | |
| 773 | 0 |
_tDevelopmental medicine and child neurology _gvol. 45 _gno. 10 _gp. 704-8 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1017/s0012162203001300 _zAvailable from publisher's website |
| 999 |
_c14276512 _d14276512 |
||