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M Pourfarzam

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Journal of Inherited Metabolic Disease|November 8, 2003

Mutation and biochemical analysis in carnitine palmitoyltransferase type II (CPT II) deficiencyS E Olpin, A Afifi, S Clark, et al.

American Journal of Human Genetics|February 11, 1999

Clear correlation of genotype with disease phenotype in very-long-chain acyl-CoA dehydrogenase deficiencyB S Andresen, S Olpin, B J Poorthuis, et al.

Journal of Inherited Metabolic Disease|October 25, 2007

Methylmalonic acidaemia: examination of genotype and biochemical data in 32 patients belonging to mut, cblA or cblB complementation groupB Merinero, B Pérez, C Pérez-Cerdá, et al.

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Search research articles

Showing results (41-50 of 43) with videos related to

Sort By:

Pageof 5

You have reached the last page of results.This site can display upto 43 results.

Journal of Inherited Metabolic Disease|November 8, 2003

Mutation and biochemical analysis in carnitine palmitoyltransferase type II (CPT II) deficiencyS E Olpin, A Afifi, S Clark, et al.

American Journal of Human Genetics|February 11, 1999

Clear correlation of genotype with disease phenotype in very-long-chain acyl-CoA dehydrogenase deficiencyB S Andresen, S Olpin, B J Poorthuis, et al.

Journal of Inherited Metabolic Disease|October 25, 2007

Methylmalonic acidaemia: examination of genotype and biochemical data in 32 patients belonging to mut, cblA or cblB complementation groupB Merinero, B Pérez, C Pérez-Cerdá, et al.

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