REFERENCES
Fenton WA, Rosenberg LE (1995) Disorders of propionate and methylmalonate metabolism. In Scriver CR, βeaudet AL, Sly WS, Valle D, eds. The Metabolic and Molecularβases of Inherited Disease, 7th edn. New York: McGraw-Hill, 1423–1499.
Fields S, Sternglanz R (1994) The two-hybrid system: an assay for protein-protein interactions. Trends Genet 10(8): 286–292.
Muro S, Pérez-Cerdá C, Rodríguez-Pombo P, et al (1999) Feasibility of DNAβased methods for prenatal diagnosis and carrier detection of propionic acidaemia. J Med Genet x36(5): 412–414.
Rodríguez-Pombo P, Hoenicka J, Muro S, et al (1998) Human propionyl-CoA carboxylase β subunit gene: exon-intron definition and mutation spectrum in Spanish and Latin American propionic acidemia patients. Am J Hum Genet 63: 360–369.
Rodríguez-Pombo P, Hoenicka J, Muro S, et al (1999) Human propionyl-CoA carboxylase β subunit gene: exon-intron deÐnition and mutation spectrum in Spanish and Latin American propionic acidemia patients. Errata. Am J Hum Genet 65: 276.
Ugarte M, Pérez-Cerdá C, Rodríguez-Pombo P, et al (1999) An overview of mutations in the PCCA and PCCB genes causing propionic acidemia. Hum Mutat 14: 275–282.
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Muro, S., Pérez, B., Rodríguez-Pombo, P. et al. Mutations affecting the β–β homomeric interaction in propionic acidaemia: An approach to the determination of the β-propionyl-CoA carboxylase functional domains. J Inherit Metab Dis 23, 300–304 (2000). https://doi.org/10.1023/A:1005617420460
Issue Date:
DOI: https://doi.org/10.1023/A:1005617420460