✦ LIBER ✦

Coding Sequence Mutations in the Alpha Subunit of Propionyl-CoA Carboxylase in Patients with Propionic Acidemia

✍ Scribed by Eric Campeau; Lucie Dupuis; Alfonso León-Del-Rio; Roy Gravel

Book ID: 115639535
Publisher: Elsevier Science
Year: 1999
Tongue: English
Weight: 244 KB
Volume: 67
Category: Article
ISSN: 1096-7192
DOI: 10.1006/mgme.1999.2850

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Immunological studies of propionyl CoA c

Immunological studies of propionyl CoA carboxylase in livers and fibroblasts of patients with propionic acidemia

✍ Chaterine McKeon; Robert Z. Eanes; R.Ray Fall; Diane M. Tasset; Barry Wolf 📂 Article 📅 1980 🏛 Elsevier Science 🌐 English ⚖ 542 KB

Mutation analysis of the propionyl-CoA c

Mutation analysis of the propionyl-CoA carboxylase α-subunit gene in four Japanese patients with propionic acidaemia

✍ T. Ohura; K. Narisawa; K. Iinuma 📂 Article 📅 1999 🏛 Springer 🌐 English ⚖ 35 KB

Human Propionyl-CoA Carboxylase β Subuni

Human Propionyl-CoA Carboxylase β Subunit Gene: Exon-Intron Definition and Mutation Spectrum in Spanish and Latin American Propionic Acidemia Patients

✍ Pilar Rodríguez-Pombo; Janet Hoenicka; Silvia Muro; Belén Pérez; Celia Pérez-Cer 📂 Article 📅 1998 🏛 American Society of Human Genetics 🌐 English ⚖ 257 KB

High Incidence of Propionic Acidemia in

High Incidence of Propionic Acidemia in Greenland Is Due to a Prevalent Mutation, 1540insCCC, in the Gene for the β-Subunit of Propionyl CoA Carboxylase

✍ Kirstine Ravn; Maja Chloupkova; Ernst Christensen; Niels Jacob Brandt; Henrik Si 📂 Article 📅 2000 🏛 American Society of Human Genetics 🌐 English ⚖ 116 KB

Correction of the Metabolic Defect in Pr

Correction of the Metabolic Defect in Propionic Acidemia Fibroblasts by Microinjection of a Full-Length cDNA or RNA Transcript Encoding the Propionyl-CoA Carboxylase β Subunit

✍ Anne-Marie Lamhonwah; Daniel Leclerc; Magali Loyer; Rino Clarizio; Roy A. Gravel 📂 Article 📅 1994 🏛 Elsevier Science 🌐 English ⚖ 469 KB

Identification of the insertion/deletion

Identification of the insertion/deletion mutation in Spanish β-propionyl-CoA carboxylase-deficient patients

✍ C. Pérez-Cerdá; P. Rodríguez-Pombo; M. Ugarte 📂 Article 📅 1994 🏛 Springer 🌐 English ⚖ 177 KB