000 01700 a2200517 4500
005 20250512200212.0
264 0 _c19840425
008 198404s 0 0 eng d
022 _a0022-510X
024 7 _a10.1016/0022-510x(83)90209-5
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aBarth, P G
245 0 0 _aAn X-linked mitochondrial disease affecting cardiac muscle, skeletal muscle and neutrophil leucocytes.
_h[electronic resource]
260 _bJournal of the neurological sciences
_cDec 1983
300 _a327-55 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article
650 0 4 _aAdenosine Triphosphatases
_xmetabolism
650 0 4 _aAdult
650 0 4 _aAged
650 0 4 _aCa(2+) Mg(2+)-ATPase
650 0 4 _aCardiomyopathies
_xdiet therapy
650 0 4 _aCarnitine
_xblood
650 0 4 _aCytochromes
_xmetabolism
650 0 4 _aFemale
650 0 4 _aGenetic Carrier Screening
650 0 4 _aGenetic Linkage
650 0 4 _aHumans
650 0 4 _aMale
650 0 4 _aMiddle Aged
650 0 4 _aMitochondria, Muscle
_xmetabolism
650 0 4 _aMuscles
_xpathology
650 0 4 _aNeutrophils
_xphysiology
650 0 4 _aOxidative Phosphorylation
650 0 4 _aPedigree
650 0 4 _aSyndrome
650 0 4 _aX Chromosome
700 1 _aScholte, H R
700 1 _aBerden, J A
700 1 _aVan der Klei-Van Moorsel, J M
700 1 _aLuyt-Houwen, I E
700 1 _aVan 't Veer-Korthof, E T
700 1 _aVan der Harten, J J
700 1 _aSobotka-Plojhar, M A
773 0 _tJournal of the neurological sciences
_gvol. 62
_gno. 1-3
_gp. 327-55
856 4 0 _uhttps://doi.org/10.1016/0022-510x(83)90209-5
_zAvailable from publisher's website
999 _c6142172
_d6142172