000 01295 a2200421 4500
005 20250513022325.0
264 0 _c19800625
008 198006s 0 0 eng d
022 _a0022-510X
024 7 _a10.1016/0022-510x(80)90165-3
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aPepin, B
245 0 0 _aFamilial mitochondrial myopathy with cataract.
_h[electronic resource]
260 _bJournal of the neurological sciences
_cMar 1980
300 _a191-203 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article
650 0 4 _aAdult
650 0 4 _aCataract
_xgenetics
650 0 4 _aChild
650 0 4 _aFemale
650 0 4 _aHLA Antigens
_xanalysis
650 0 4 _aHumans
650 0 4 _aMale
650 0 4 _aMicroscopy, Electron
650 0 4 _aMiddle Aged
650 0 4 _aMitochondria, Muscle
650 0 4 _aMuscles
_xpathology
650 0 4 _aMuscular Diseases
_xgenetics
650 0 4 _aOphthalmoplegia
_xgenetics
650 0 4 _aPedigree
650 0 4 _aSyndrome
700 1 _aMikol, J
700 1 _aGoldstein, B
700 1 _aAron, J J
700 1 _aLebuisson, D A
773 0 _tJournal of the neurological sciences
_gvol. 45
_gno. 2-3
_gp. 191-203
856 4 0 _uhttps://doi.org/10.1016/0022-510x(80)90165-3
_zAvailable from publisher's website
999 _c7365008
_d7365008