| 000 | 01637 a2200529 4500 | ||
|---|---|---|---|
| 005 | 20250518083330.0 | ||
| 264 | 0 | _c20210705 | |
| 008 | 202107s 0 0 eng d | ||
| 022 | _a1460-2083 | ||
| 024 | 7 |
_a10.1093/hmg/ddaa020 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aGutiérrez Cortés, Nicolás | |
| 245 | 0 | 0 |
_aMutation m.3395A > G in MT-ND1 leads to variable pathologic manifestations. _h[electronic resource] |
| 260 |
_bHuman molecular genetics _c04 2020 |
||
| 300 |
_a980-989 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 | _aChild |
| 650 | 0 | 4 | _aChild, Preschool |
| 650 | 0 | 4 |
_aDNA, Mitochondrial _xanalysis |
| 650 | 0 | 4 |
_aDeafness _xclassification |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aInfant |
| 650 | 0 | 4 | _aInfant, Newborn |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aMiddle Aged |
| 650 | 0 | 4 |
_aMitochondria _xgenetics |
| 650 | 0 | 4 | _aMutation |
| 650 | 0 | 4 |
_aNADH Dehydrogenase _xgenetics |
| 700 | 1 | _aPertuiset, Claire | |
| 700 | 1 | _aDumon, Elodie | |
| 700 | 1 | _aBörlin, Marine | |
| 700 | 1 | _aDa Costa, Barbara | |
| 700 | 1 | _aLe Guédard, Marina | |
| 700 | 1 | _aStojkovic, Tanya | |
| 700 | 1 | _aLoundon, Natalie | |
| 700 | 1 | _aRouillon, Isabelle | |
| 700 | 1 | _aNadjar, Yann | |
| 700 | 1 | _aLetellier, Thierry | |
| 700 | 1 | _aJonard, Laurence | |
| 700 | 1 | _aMarlin, Sandrine | |
| 700 | 1 | _aRocher, Christophe | |
| 773 | 0 |
_tHuman molecular genetics _gvol. 29 _gno. 6 _gp. 980-989 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1093/hmg/ddaa020 _zAvailable from publisher's website |
| 999 |
_c30589622 _d30589622 |
||