| 000 | 01188 a2200325 4500 | ||
|---|---|---|---|
| 005 | 20250514065303.0 | ||
| 264 | 0 | _c20030722 | |
| 008 | 200307s 0 0 eng d | ||
| 022 | _a0002-9297 | ||
| 024 | 7 |
_a10.1086/375656 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aSun, Fengzhu | |
| 245 | 0 | 0 |
_aA novel class of tests for the detection of mitochondrial DNA-mutation involvement in diseases. _h[electronic resource] |
| 260 |
_bAmerican journal of human genetics _cJun 2003 |
||
| 300 |
_a1515-26 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, U.S. Gov't, P.H.S. | ||
| 650 | 0 | 4 |
_aDNA Mutational Analysis _xmethods |
| 650 | 0 | 4 |
_aDNA, Mitochondrial _xgenetics |
| 650 | 0 | 4 |
_aDiabetes Mellitus, Type 2 _xgenetics |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 |
_aHypertension _xgenetics |
| 650 | 0 | 4 | _aModels, Genetic |
| 650 | 0 | 4 |
_aOptic Atrophy, Hereditary, Leber _xgenetics |
| 650 | 0 | 4 | _aPedigree |
| 700 | 1 | _aCui, Jing | |
| 700 | 1 | _aGavras, Haralambos | |
| 700 | 1 | _aSchwartz, Faina | |
| 773 | 0 |
_tAmerican journal of human genetics _gvol. 72 _gno. 6 _gp. 1515-26 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1086/375656 _zAvailable from publisher's website |
| 999 |
_c12519916 _d12519916 |
||