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K D Gerbitz

Showing results (61-70 of 63) with videos related to

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Journal of Inherited Metabolic Disease|May 10, 2002
Screening for carnitine palmitoyltransferase II deficiency by tandem mass spectrometryK Gempel, S Kiechl, S Hofmann, et al.
Annals of Neurology|August 12, 1999
Loss-of-function mutations of SURF-1 are specifically associated with Leigh syndrome with cytochrome c oxidase deficiencyV Tiranti, M Jaksch, S Hofmann, et al.
Neurology|October 24, 2001
Homozygosity (E140K) in SCO2 causes delayed infantile onset of cardiomyopathy and neuropathyM Jaksch, R Horvath, N Horn, et al.
Pageof 7

Showing results (61-70 of 63) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 63 results.
Journal of Inherited Metabolic Disease|May 10, 2002
Screening for carnitine palmitoyltransferase II deficiency by tandem mass spectrometryK Gempel, S Kiechl, S Hofmann, et al.
Annals of Neurology|August 12, 1999
Loss-of-function mutations of SURF-1 are specifically associated with Leigh syndrome with cytochrome c oxidase deficiencyV Tiranti, M Jaksch, S Hofmann, et al.
Neurology|October 24, 2001
Homozygosity (E140K) in SCO2 causes delayed infantile onset of cardiomyopathy and neuropathyM Jaksch, R Horvath, N Horn, et al.
Pageof 7