Your search returned 3 results.

Results
	1.	Gene structure and mutations of glutaryl-coenzyme A dehydrogenase: impaired association of enzyme subunits that is due to an A421V substitution causes glutaric acidemia type I in the Amish. [electronic resource] by Biery, B J Stein, D E Morton, D H Goodman, S I Producer: 19961211 In: American journal of human genetics vol. 59 Availability: No items available. Save to lists Add to cart (remove)
	2.	Cloning of glutaryl-CoA dehydrogenase cDNA, and expression of wild type and mutant enzymes in Escherichia coli. [electronic resource] by Goodman, S I Kratz, L E DiGiulio, K A Biery, B J Goodman, K E Isaya, G Frerman, F E Producer: 19960214 In: Human molecular genetics vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Identification of the alpha-aminoadipic semialdehyde synthase gene, which is defective in familial hyperlysinemia. [electronic resource] by Sacksteder, K A Biery, B J Morrell, J C Goodman, B K Geisbrecht, B V Cox, R P Gould, S J Geraghty, M T Producer: 20010607 In: American journal of human genetics vol. 66 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

Refine your search