Kedishvili NY, Popov KM, Harris RA (Oct 1991). "The effect of ligand binding on the proteolytic pattern of methylmalonate semialdehyde dehydrogenase". Archives of Biochemistry and Biophysics. 290 (1): 21–6. doi:10.1016/0003-9861(91)90586-8. PMID1898092.
Pollitt RJ, Green A, Smith R (1985). "Excessive excretion of beta-alanine and of 3-hydroxypropionic, R- and S-3-aminoisobutyric, R- and S-3-hydroxyisobutyric and S-2-(hydroxymethyl)butyric acids probably due to a defect in the metabolism of the corresponding malonic semialdehydes". Journal of Inherited Metabolic Disease. 8 (2): 75–9. doi:10.1007/bf01801669. PMID3939535. S2CID6335599.
Gray RG, Pollitt RJ, Webley J (Aug 1987). "Methylmalonic semialdehyde dehydrogenase deficiency: demonstration of defective valine and beta-alanine metabolism and reduced malonic semialdehyde dehydrogenase activity in cultured fibroblasts". Biochemical Medicine and Metabolic Biology. 38 (1): 121–4. doi:10.1016/0885-4505(87)90069-7. PMID3117077.
Shield JP, Gough R, Allen J, Newbury-Ecob R (Jul 2001). "3-Hydroxyisobutyric aciduria: phenotypic heterogeneity within a single family". Clinical Dysmorphology. 10 (3): 189–91. doi:10.1097/00019605-200107000-00007. PMID11446412.
Sass JO, Walter M, Shield JP, Atherton AM, Garg U, Scott D, Woods CG, Smith LD (May 2012). "3-Hydroxyisobutyrate aciduria and mutations in the ALDH6A1 gene coding for methylmalonate semialdehyde dehydrogenase". Journal of Inherited Metabolic Disease. 35 (3): 437–42. doi:10.1007/s10545-011-9381-x. PMID21863277. S2CID6911924.
Kedishvili NY, Popov KM, Harris RA (Oct 1991). "The effect of ligand binding on the proteolytic pattern of methylmalonate semialdehyde dehydrogenase". Archives of Biochemistry and Biophysics. 290 (1): 21–6. doi:10.1016/0003-9861(91)90586-8. PMID1898092.
Pollitt RJ, Green A, Smith R (1985). "Excessive excretion of beta-alanine and of 3-hydroxypropionic, R- and S-3-aminoisobutyric, R- and S-3-hydroxyisobutyric and S-2-(hydroxymethyl)butyric acids probably due to a defect in the metabolism of the corresponding malonic semialdehydes". Journal of Inherited Metabolic Disease. 8 (2): 75–9. doi:10.1007/bf01801669. PMID3939535. S2CID6335599.
Gray RG, Pollitt RJ, Webley J (Aug 1987). "Methylmalonic semialdehyde dehydrogenase deficiency: demonstration of defective valine and beta-alanine metabolism and reduced malonic semialdehyde dehydrogenase activity in cultured fibroblasts". Biochemical Medicine and Metabolic Biology. 38 (1): 121–4. doi:10.1016/0885-4505(87)90069-7. PMID3117077.
Shield JP, Gough R, Allen J, Newbury-Ecob R (Jul 2001). "3-Hydroxyisobutyric aciduria: phenotypic heterogeneity within a single family". Clinical Dysmorphology. 10 (3): 189–91. doi:10.1097/00019605-200107000-00007. PMID11446412.
Sass JO, Walter M, Shield JP, Atherton AM, Garg U, Scott D, Woods CG, Smith LD (May 2012). "3-Hydroxyisobutyrate aciduria and mutations in the ALDH6A1 gene coding for methylmalonate semialdehyde dehydrogenase". Journal of Inherited Metabolic Disease. 35 (3): 437–42. doi:10.1007/s10545-011-9381-x. PMID21863277. S2CID6911924.
ncbi.nlm.nih.gov
"Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
"Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
Chambliss KL, Gray RG, Rylance G, Pollitt RJ, Gibson KM (Jul 2000). "Molecular characterization of methylmalonate semialdehyde dehydrogenase deficiency". Journal of Inherited Metabolic Disease. 23 (5): 497–504. doi:10.1023/A:1005616315087. PMID10947204. S2CID9714122.
Pollitt RJ, Green A, Smith R (1985). "Excessive excretion of beta-alanine and of 3-hydroxypropionic, R- and S-3-aminoisobutyric, R- and S-3-hydroxyisobutyric and S-2-(hydroxymethyl)butyric acids probably due to a defect in the metabolism of the corresponding malonic semialdehydes". Journal of Inherited Metabolic Disease. 8 (2): 75–9. doi:10.1007/bf01801669. PMID3939535. S2CID6335599.
Sass JO, Walter M, Shield JP, Atherton AM, Garg U, Scott D, Woods CG, Smith LD (May 2012). "3-Hydroxyisobutyrate aciduria and mutations in the ALDH6A1 gene coding for methylmalonate semialdehyde dehydrogenase". Journal of Inherited Metabolic Disease. 35 (3): 437–42. doi:10.1007/s10545-011-9381-x. PMID21863277. S2CID6911924.