B. Biery

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.

D. Morton, S. Goodman, B. Biery, 1996, American journal of human genetics.

Identification of the alpha-aminoadipic semialdehyde synthase gene, which is defective in familial hyperlysinemia.

R P Cox, B. Geisbrecht, S. Gould, 2000, American journal of human genetics.

Cloning of glutaryl-CoA dehydrogenase cDNA, and expression of wild type and mutant enzymes in Escherichia coli.

K. Goodman, F. Frerman, S. Goodman, 1995, Human molecular genetics.

Hyperornithinaemia-hyperammonaemia-homocitrullinuria syndrome is caused by mutations in a gene encoding a mitochondrial ornithine transporter

S. Almashanu, C. Obie, D. Valle, 1999, Nature Genetics.

Glutaric acidemia (type I)

S. Goodman, B. Biery, 2017 .