| 000 | 00967 a2200277 4500 | ||
|---|---|---|---|
| 005 | 20250513150725.0 | ||
| 264 | 0 | _c19981130 | |
| 008 | 199811s 0 0 eng d | ||
| 022 | _a0141-8955 | ||
| 024 | 7 |
_a10.1023/a:1005357221101 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aChinnery, P F | |
| 245 | 0 | 0 |
_aMitochondrial genotype and clinical phenotype. _h[electronic resource] |
| 260 |
_bJournal of inherited metabolic disease _cJun 1998 |
||
| 300 |
_a321-5 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't; Review | ||
| 650 | 0 | 4 | _aDNA, Mitochondrial |
| 650 | 0 | 4 | _aGenotype |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 |
_aMetabolism, Inborn Errors _xgenetics |
| 650 | 0 | 4 | _aMitochondria |
| 650 | 0 | 4 | _aPhenotype |
| 700 | 1 | _aTurnbull, D M | |
| 773 | 0 |
_tJournal of inherited metabolic disease _gvol. 21 _gno. 4 _gp. 321-5 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1023/a:1005357221101 _zAvailable from publisher's website |
| 999 |
_c9666214 _d9666214 |
||