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