| 000 | 01722 a2200529 4500 | ||
|---|---|---|---|
| 005 | 20250513033620.0 | ||
| 264 | 0 | _c19950807 | |
| 008 | 199508s 0 0 eng d | ||
| 022 | _a0006-3002 | ||
| 024 | 7 |
_a10.1016/0925-4439(95)00020-5 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aMorgan-Hughes, J A | |
| 245 | 0 | 0 |
_aMitochondrial DNA (mtDNA) diseases: correlation of genotype to phenotype. _h[electronic resource] |
| 260 |
_bBiochimica et biophysica acta _cMay 1995 |
||
| 300 |
_a135-40 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 | _aAdolescent |
| 650 | 0 | 4 | _aAdult |
| 650 | 0 | 4 | _aAge of Onset |
| 650 | 0 | 4 | _aBiopsy |
| 650 | 0 | 4 | _aChild |
| 650 | 0 | 4 |
_aCytochrome b Group _xgenetics |
| 650 | 0 | 4 |
_aDNA, Mitochondrial _xgenetics |
| 650 | 0 | 4 |
_aElectron Transport Complex III _xgenetics |
| 650 | 0 | 4 |
_aElectron Transport Complex IV _xgenetics |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aGenotype |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 |
_aMELAS Syndrome _xgenetics |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aMiddle Aged |
| 650 | 0 | 4 |
_aMitochondrial Encephalomyopathies _xgenetics |
| 650 | 0 | 4 |
_aMuscle, Skeletal _xmetabolism |
| 650 | 0 | 4 |
_aNAD(P)H Dehydrogenase (Quinone) _xgenetics |
| 650 | 0 | 4 | _aPhenotype |
| 650 | 0 | 4 | _aPoint Mutation |
| 650 | 0 | 4 |
_aRNA, Transfer, Leu _xgenetics |
| 700 | 1 | _aSweeney, M G | |
| 700 | 1 | _aCooper, J M | |
| 700 | 1 | _aHammans, S R | |
| 700 | 1 | _aBrockington, M | |
| 700 | 1 | _aSchapira, A H | |
| 700 | 1 | _aHarding, A E | |
| 700 | 1 | _aClark, J B | |
| 773 | 0 |
_tBiochimica et biophysica acta _gvol. 1271 _gno. 1 _gp. 135-40 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1016/0925-4439(95)00020-5 _zAvailable from publisher's website |
| 999 |
_c7598638 _d7598638 |
||