000 01250 a2200385 4500
005 20250513120819.0
264 0 _c19970729
008 199707s 0 0 eng d
022 _a0964-6906
024 7 _a10.1093/hmg/6.6.935
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aTaanman, J W
245 0 0 _aMolecular mechanisms in mitochondrial DNA depletion syndrome.
_h[electronic resource]
260 _bHuman molecular genetics
_cJun 1997
300 _a935-42 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aCell Nucleus
650 0 4 _aCells, Cultured
650 0 4 _aDNA, Mitochondrial
650 0 4 _aElectron Transport Complex IV
_xgenetics
650 0 4 _aFluorescent Antibody Technique, Indirect
650 0 4 _aGenetic Complementation Test
650 0 4 _aHumans
650 0 4 _aInfant
650 0 4 _aMale
650 0 4 _aSyndrome
700 1 _aBodnar, A G
700 1 _aCooper, J M
700 1 _aMorris, A A
700 1 _aClayton, P T
700 1 _aLeonard, J V
700 1 _aSchapira, A H
773 0 _tHuman molecular genetics
_gvol. 6
_gno. 6
_gp. 935-42
856 4 0 _uhttps://doi.org/10.1093/hmg/6.6.935
_zAvailable from publisher's website
999 _c9156815
_d9156815