000 01318 a2200397 4500
005 20250514170711.0
264 0 _c20040824
008 200408s 0 0 eng d
022 _a0141-8955
024 7 _a10.1023/b:boli.0000010003.14113.af
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aBudde, S M S
245 0 0 _aClinical heterogeneity in patients with mutations in the NDUFS4 gene of mitochondrial complex I.
_h[electronic resource]
260 _bJournal of inherited metabolic disease
_c2003
300 _a813-5 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aElectron Transport Complex I
650 0 4 _aFemale
650 0 4 _aGenotype
650 0 4 _aHumans
650 0 4 _aInfant
650 0 4 _aMale
650 0 4 _aMutation
650 0 4 _aNADH Dehydrogenase
650 0 4 _aNADH, NADPH Oxidoreductases
_xgenetics
700 1 _avan den Heuvel, L P W J
700 1 _aSmeets, R J P
700 1 _aSkladal, D
700 1 _aMayr, J A
700 1 _aBoelen, C
700 1 _aPetruzzella, V
700 1 _aPapa, S
700 1 _aSmeitink, J A M
773 0 _tJournal of inherited metabolic disease
_gvol. 26
_gno. 8
_gp. 813-5
856 4 0 _uhttps://doi.org/10.1023/b:boli.0000010003.14113.af
_zAvailable from publisher's website
999 _c14489100
_d14489100