The c.419-420insA in the MTP gene is associated with abetalipoproteinemia among French-Canadians
- 17 December 2003
- journal article
- research article
- Published by Elsevier in Molecular Genetics and Metabolism
- Vol. 81 (2) , 140-143
- https://doi.org/10.1016/j.ymgme.2003.11.001
Abstract
No abstract availableKeywords
This publication has 19 references indexed in Scilit:
- Effect of the factor VII R353Q missense mutation on plasma apolipoprotein B levels: impact of visceral obesityJournal of Human Genetics, 2003
- The interleukin 6 −174G/C Polymorphism is associated with indices of obesity in menJournal of Human Genetics, 2003
- Effects of the FABP2 A54T Mutation on Triglyceride Metabolism of Viscerally Obese MenObesity Research, 2001
- Microsomal triglyceride transfer protein (MTP) gene mutations in Canadian subjects with abetalipoproteinemiaHuman Mutation, 2000
- Abetalipoproteinemia Caused by Maternal Isodisomy of Chromosome 4q Containing an Intron 9 Splice Acceptor Mutation in the Microsomal Triglyceride Transfer Protein GeneArteriosclerosis, Thrombosis, and Vascular Biology, 1999
- The use of a highly informative CA repeat polymorphism within the abetalipoproteinaemia locus (4q22–24)Prenatal Diagnosis, 1997
- A Novel Abetalipoproteinemia GenotypeJournal of Biological Chemistry, 1996
- Abetalipoproteinemia. New insights into lipoprotein assembly and vitamin E metabolism from a rare genetic diseaseJAMA, 1993
- Absence of Microsomal Triglyceride Transfer Protein in Individuals with AbetalipoproteinemiaScience, 1992
- AbetalipoproteinemiaArchives of Neurology, 1980