000 01287 a2200397 4500
005 20250514031800.0
264 0 _c20020503
008 200205s 0 0 eng d
022 _a0009-9147
040 _aNLM
_beng
_cNLM
100 1 _aSchuelke, Markus
245 0 0 _aNew nuclear encoded mitochondrial mutation illustrates pitfalls in prenatal diagnosis by biochemical methods.
_h[electronic resource]
260 _bClinical chemistry
_cMay 2002
300 _a772-5 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aAcidosis, Lactic
_xcongenital
650 0 4 _aElectron Transport Complex I
650 0 4 _aFemale
650 0 4 _aHumans
650 0 4 _aMale
650 0 4 _aMitochondria
_xgenetics
650 0 4 _aNADH Dehydrogenase
650 0 4 _aNADH, NADPH Oxidoreductases
_xdeficiency
650 0 4 _aPedigree
650 0 4 _aPregnancy
650 0 4 _aPrenatal Diagnosis
_xmethods
650 0 4 _aProteins
_xgenetics
700 1 _aDetjen, Anne
700 1 _avan den Heuvel, Lambert
700 1 _aKorenke, Christoph
700 1 _aJanssen, Antoon
700 1 _aSmits, Arie
700 1 _aTrijbels, Frans
700 1 _aSmeitink, Jan
773 0 _tClinical chemistry
_gvol. 48
_gno. 5
_gp. 772-5
999 _c11879117
_d11879117