000 01537 a2200457 4500
005 20250515050351.0
264 0 _c20061227
008 200612s 0 0 eng d
022 _a1526-632X
024 7 _a10.1212/01.wnl.0000244435.27645.54
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aMorava, E
245 0 0 _aMitochondrial disease criteria: diagnostic applications in children.
_h[electronic resource]
260 _bNeurology
_cNov 2006
300 _a1823-6 p.
_bdigital
500 _aPublication Type: Comparative Study; Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aBiopsy
_xstandards
650 0 4 _aChild
650 0 4 _aDNA Mutational Analysis
_xmethods
650 0 4 _aDNA, Mitochondrial
_xanalysis
650 0 4 _aDiagnosis, Differential
650 0 4 _aFemale
650 0 4 _aGenetic Predisposition to Disease
_xgenetics
650 0 4 _aGenetic Testing
_xmethods
650 0 4 _aHumans
650 0 4 _aMale
650 0 4 _aMitochondria
_xgenetics
650 0 4 _aMitochondrial Diseases
_xdiagnosis
650 0 4 _aMuscle, Skeletal
_xmetabolism
650 0 4 _aMuscular Diseases
_xdiagnosis
650 0 4 _aMutation
_xgenetics
650 0 4 _aPredictive Value of Tests
700 1 _avan den Heuvel, L
700 1 _aHol, F
700 1 _ade Vries, M C
700 1 _aHogeveen, M
700 1 _aRodenburg, R J
700 1 _aSmeitink, J A M
773 0 _tNeurology
_gvol. 67
_gno. 10
_gp. 1823-6
856 4 0 _uhttps://doi.org/10.1212/01.wnl.0000244435.27645.54
_zAvailable from publisher's website
999 _c16701186
_d16701186