| 000 | 01372 a2200409 4500 | ||
|---|---|---|---|
| 005 | 20250515030400.0 | ||
| 264 | 0 | _c20061215 | |
| 008 | 200612s 0 0 eng d | ||
| 022 | _a1468-6244 | ||
| 024 | 7 |
_a10.1136/jmg.2006.042168 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aHinttala, R | |
| 245 | 0 | 0 |
_aAnalysis of mitochondrial DNA sequences in patients with isolated or combined oxidative phosphorylation system deficiency. _h[electronic resource] |
| 260 |
_bJournal of medical genetics _cNov 2006 |
||
| 300 |
_a881-6 p. _bdigital |
||
| 500 | _aPublication Type: Evaluation Study; Letter; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 | _aAdolescent |
| 650 | 0 | 4 | _aChild |
| 650 | 0 | 4 | _aChild, Preschool |
| 650 | 0 | 4 | _aComputational Biology |
| 650 | 0 | 4 | _aDNA Mutational Analysis |
| 650 | 0 | 4 |
_aDNA, Mitochondrial _xchemistry |
| 650 | 0 | 4 |
_aGenetic Testing _xmethods |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aInfant |
| 650 | 0 | 4 | _aInfant, Newborn |
| 650 | 0 | 4 |
_aMitochondrial Diseases _xdiagnosis |
| 650 | 0 | 4 | _aPhylogeny |
| 700 | 1 | _aSmeets, R | |
| 700 | 1 | _aMoilanen, J S | |
| 700 | 1 | _aUgalde, C | |
| 700 | 1 | _aUusimaa, J | |
| 700 | 1 | _aSmeitink, J A M | |
| 700 | 1 | _aMajamaa, K | |
| 773 | 0 |
_tJournal of medical genetics _gvol. 43 _gno. 11 _gp. 881-6 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1136/jmg.2006.042168 _zAvailable from publisher's website |
| 999 |
_c16334898 _d16334898 |
||