000 | 01667 a2200565 4500 | ||
---|---|---|---|
005 | 20250515104349.0 | ||
264 | 0 | _c20080207 | |
008 | 200802s 0 0 eng d | ||
022 | _a1098-1004 | ||
024 | 7 |
_a10.1002/humu.9519 _2doi |
|
040 |
_aNLM _beng _cNLM |
||
100 | 1 | _aDimmock, D P | |
245 | 0 | 0 |
_aClinical and molecular features of mitochondrial DNA depletion due to mutations in deoxyguanosine kinase. _h[electronic resource] |
260 |
_bHuman mutation _cFeb 2008 |
||
300 |
_a330-1 p. _bdigital |
||
500 | _aPublication Type: Journal Article; Research Support, N.I.H., Extramural | ||
650 | 0 | 4 | _aAdolescent |
650 | 0 | 4 | _aChild, Preschool |
650 | 0 | 4 |
_aDNA, Mitochondrial _xgenetics |
650 | 0 | 4 | _aFemale |
650 | 0 | 4 | _aHumans |
650 | 0 | 4 | _aInfant |
650 | 0 | 4 | _aInfant, Newborn |
650 | 0 | 4 | _aMale |
650 | 0 | 4 |
_aMutation _xgenetics |
650 | 0 | 4 | _aOrgan Specificity |
650 | 0 | 4 |
_aPhosphotransferases (Alcohol Group Acceptor) _xgenetics |
700 | 1 | _aZhang, Q | |
700 | 1 | _aDionisi-Vici, C | |
700 | 1 | _aCarrozzo, R | |
700 | 1 | _aShieh, J | |
700 | 1 | _aTang, L-Y | |
700 | 1 | _aTruong, C | |
700 | 1 | _aSchmitt, E | |
700 | 1 | _aSifry-Platt, M | |
700 | 1 | _aLucioli, S | |
700 | 1 | _aSantorelli, F M | |
700 | 1 | _aFicicioglu, C H | |
700 | 1 | _aRodriguez, M | |
700 | 1 | _aWierenga, K | |
700 | 1 | _aEnns, G M | |
700 | 1 | _aLongo, N | |
700 | 1 | _aLipson, M H | |
700 | 1 | _aVallance, H | |
700 | 1 | _aCraigen, W J | |
700 | 1 | _aScaglia, F | |
700 | 1 | _aWong, L-J | |
773 | 0 |
_tHuman mutation _gvol. 29 _gno. 2 _gp. 330-1 |
|
856 | 4 | 0 |
_uhttps://doi.org/10.1002/humu.9519 _zAvailable from publisher's website |
999 |
_c17713085 _d17713085 |