000 01517 a2200457 4500
005 20250511175459.0
264 0 _c19930527
008 199305s 0 0 eng d
022 _a0960-8966
024 7 _a10.1016/s0960-8966(06)80003-9
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aLombès, A
245 0 0 _aAnalysis of the tissue distribution and inheritance of heteroplasmic mitochondrial DNA point mutation by denaturing gradient gel electrophoresis in MERRF syndrome.
_h[electronic resource]
260 _bNeuromuscular disorders : NMD
_c1992
300 _a323-30 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aAdolescent
650 0 4 _aAdult
650 0 4 _aAged
650 0 4 _aBase Sequence
650 0 4 _aChild
650 0 4 _aDNA Mutational Analysis
650 0 4 _aDNA, Mitochondrial
_xgenetics
650 0 4 _aElectrophoresis
_xmethods
650 0 4 _aFemale
650 0 4 _aHistocytochemistry
650 0 4 _aHumans
650 0 4 _aMERRF Syndrome
_xgenetics
650 0 4 _aMale
650 0 4 _aMolecular Sequence Data
650 0 4 _aMuscles
_xchemistry
650 0 4 _aNucleic Acid Denaturation
650 0 4 _aPhenotype
650 0 4 _aPoint Mutation
700 1 _aDiaz, C
700 1 _aRomero, N B
700 1 _aZiegler, F
700 1 _aFardeau, M
773 0 _tNeuromuscular disorders : NMD
_gvol. 2
_gno. 5-6
_gp. 323-30
856 4 0 _uhttps://doi.org/10.1016/s0960-8966(06)80003-9
_zAvailable from publisher's website
999 _c1306707
_d1306707