000 01432 a2200397 4500
005 20250513185751.0
264 0 _c19990902
008 199909s 0 0 spa d
022 _a0034-8376
040 _aNLM
_beng
_cNLM
100 1 _aBarrera-Ramírez, C F
245 0 0 _a[The other genome: the clinical concept of mitochondrial cytopathies or disorders of pxidative phosphorylation].
_h[electronic resource]
260 _bRevista de investigacion clinica; organo del Hospital de Enfermedades de la Nutricion
_c
300 _a121-34 p.
_bdigital
500 _aPublication Type: English Abstract; Journal Article; Review
650 0 4 _aCardiomyopathies
_xgenetics
650 0 4 _aDNA, Mitochondrial
_xgenetics
650 0 4 _aDiagnosis, Differential
650 0 4 _aExtrachromosomal Inheritance
650 0 4 _aFemale
650 0 4 _aGenome
650 0 4 _aHumans
650 0 4 _aLactic Acid
_xblood
650 0 4 _aMale
650 0 4 _aMitochondrial Myopathies
_xdiagnosis
650 0 4 _aOptic Atrophies, Hereditary
_xgenetics
650 0 4 _aOxidative Phosphorylation
650 0 4 _aPhenotype
650 0 4 _aPyruvic Acid
_xblood
700 1 _aBarragán-Campos, H M
700 1 _aSánchez-Guerrero, J
700 1 _aGarcía-Ramos, G
700 1 _aVega-Boada, F
700 1 _aEstañol, B
773 0 _tRevista de investigacion clinica; organo del Hospital de Enfermedades de la Nutricion
_gvol. 51
_gno. 2
_gp. 121-34
999 _c10368691
_d10368691