000 01541 a2200409 4500
005 20250513190325.0
264 0 _c19990920
008 199909s 0 0 eng d
022 _a0022-510X
024 7 _a10.1016/s0022-510x(99)00088-x
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aCock, H R
245 0 0 _aFunctional consequences of the 3460-bp mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy.
_h[electronic resource]
260 _bJournal of the neurological sciences
_cMay 1999
300 _a10-7 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aAdenosine Triphosphate
_xbiosynthesis
650 0 4 _aAdult
650 0 4 _aDNA, Mitochondrial
_xgenetics
650 0 4 _aElectron Transport
_xgenetics
650 0 4 _aElectron Transport Complex I
650 0 4 _aFibroblasts
650 0 4 _aHumans
650 0 4 _aMiddle Aged
650 0 4 _aMitochondria, Muscle
_xchemistry
650 0 4 _aMutation
_xgenetics
650 0 4 _aNAD
_xmetabolism
650 0 4 _aNADH, NADPH Oxidoreductases
_xbiosynthesis
650 0 4 _aOptic Atrophies, Hereditary
_xgenetics
650 0 4 _aReverse Transcriptase Polymerase Chain Reaction
650 0 4 _aRotenone
_xpharmacology
650 0 4 _aUncoupling Agents
_xpharmacology
700 1 _aCooper, J M
700 1 _aSchapira, A H
773 0 _tJournal of the neurological sciences
_gvol. 165
_gno. 1
_gp. 10-7
856 4 0 _uhttps://doi.org/10.1016/s0022-510x(99)00088-x
_zAvailable from publisher's website
999 _c10384081
_d10384081