000 01420 a2200445 4500
005 20250513095624.0
264 0 _c19960917
008 199609s 0 0 eng d
022 _a0340-6199
024 7 _a10.1007/BF02002711
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aMunnich, A
245 0 0 _aClinical presentations and laboratory investigations in respiratory chain deficiency.
_h[electronic resource]
260 _bEuropean journal of pediatrics
_cApr 1996
300 _a262-74 p.
_bdigital
500 _aPublication Type: Journal Article; Review
650 0 4 _aChild, Preschool
650 0 4 _aDNA, Mitochondrial
_xgenetics
650 0 4 _aDiagnosis, Differential
650 0 4 _aElectron Transport
_xgenetics
650 0 4 _aEnzymes
_xdeficiency
650 0 4 _aFemale
650 0 4 _aGenetic Counseling
650 0 4 _aHumans
650 0 4 _aInfant
650 0 4 _aInfant, Newborn
650 0 4 _aMale
650 0 4 _aMitochondrial Encephalomyopathies
_xdiagnosis
650 0 4 _aMitochondrial Myopathies
_xdiagnosis
650 0 4 _aPhenotype
650 0 4 _aPrenatal Diagnosis
650 0 4 _aPrognosis
700 1 _aRötig, A
700 1 _aChretien, D
700 1 _aSaudubray, J M
700 1 _aCormier, V
700 1 _aRustin, P
773 0 _tEuropean journal of pediatrics
_gvol. 155
_gno. 4
_gp. 262-74
856 4 0 _uhttps://doi.org/10.1007/BF02002711
_zAvailable from publisher's website
999 _c8774673
_d8774673