000 01466 a2200457 4500
005 20250511202450.0
264 0 _c19920302
008 199203s 0 0 eng d
022 _a0028-3878
024 7 _a10.1212/wnl.42.1.209
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aTritschler, H J
245 0 0 _aMitochondrial myopathy of childhood associated with depletion of mitochondrial DNA.
_h[electronic resource]
260 _bNeurology
_cJan 1992
300 _a209-17 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
650 0 4 _aBlotting, Southern
650 0 4 _aChild, Preschool
650 0 4 _aDNA, Mitochondrial
_xanalysis
650 0 4 _aFemale
650 0 4 _aHistocytochemistry
650 0 4 _aHumans
650 0 4 _aImmunohistochemistry
650 0 4 _aInfant
650 0 4 _aMale
650 0 4 _aMitochondria, Muscle
_xmetabolism
650 0 4 _aMuscles
_xmetabolism
650 0 4 _aMuscular Diseases
_xgenetics
650 0 4 _aNucleic Acid Hybridization
700 1 _aAndreetta, F
700 1 _aMoraes, C T
700 1 _aBonilla, E
700 1 _aArnaudo, E
700 1 _aDanon, M J
700 1 _aGlass, S
700 1 _aZelaya, B M
700 1 _aVamos, E
700 1 _aTelerman-Toppet, N
773 0 _tNeurology
_gvol. 42
_gno. 1
_gp. 209-17
856 4 0 _uhttps://doi.org/10.1212/wnl.42.1.209
_zAvailable from publisher's website
999 _c1740701
_d1740701