| 000 | 01573 a2200481 4500 | ||
|---|---|---|---|
| 005 | 20250515150958.0 | ||
| 264 | 0 | _c20090204 | |
| 008 | 200902s 0 0 eng d | ||
| 022 | _a1932-6203 | ||
| 024 | 7 |
_a10.1371/journal.pone.0003815 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aWeissman, Jacqueline R | |
| 245 | 0 | 0 |
_aMitochondrial disease in autism spectrum disorder patients: a cohort analysis. _h[electronic resource] |
| 260 |
_bPloS one _c2008 |
||
| 300 |
_ae3815 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 | _aAdolescent |
| 650 | 0 | 4 |
_aAutistic Disorder _xclassification |
| 650 | 0 | 4 | _aChild |
| 650 | 0 | 4 | _aChild, Preschool |
| 650 | 0 | 4 | _aCohort Studies |
| 650 | 0 | 4 |
_aDNA, Mitochondrial _xgenetics |
| 650 | 0 | 4 | _aDiagnosis, Differential |
| 650 | 0 | 4 |
_aElectron Transport Complex I _xdeficiency |
| 650 | 0 | 4 |
_aElectron Transport Complex III _xdeficiency |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 |
_aMitochondrial Diseases _xcomplications |
| 650 | 0 | 4 | _aMutation |
| 650 | 0 | 4 | _aOxidative Phosphorylation |
| 650 | 0 | 4 | _aPhenotype |
| 650 | 0 | 4 | _aYoung Adult |
| 700 | 1 | _aKelley, Richard I | |
| 700 | 1 | _aBauman, Margaret L | |
| 700 | 1 | _aCohen, Bruce H | |
| 700 | 1 | _aMurray, Katherine F | |
| 700 | 1 | _aMitchell, Rebecca L | |
| 700 | 1 | _aKern, Rebecca L | |
| 700 | 1 | _aNatowicz, Marvin R | |
| 773 | 0 |
_tPloS one _gvol. 3 _gno. 11 _gp. e3815 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1371/journal.pone.0003815 _zAvailable from publisher's website |
| 999 |
_c18498623 _d18498623 |
||