Molecular and functional analysis of two new MTTP gene mutations in an atypical case of abetalipoproteinemia-Reference-Cited by-同舟云学术

Molecular and functional analysis of two new MTTP gene mutations in an atypical case of abetalipoproteinemia

Published:2012-03 Issue:3 Volume:53 Page:548-555
ISSN:0022-2275
Container-title:Journal of Lipid Research
language:en
Short-container-title:Journal of Lipid Research

Author:

Di Filippo Mathilde,Créhalet Hervé,Samson-Bouma Marie Elisabeth,Bonnet Véronique,Aggerbeck Lawrence P.,Rabès Jean-Pierre,Gottrand Frederic,Luc Gérald,Bozon Dominique,Sassolas Agnès

Publisher

Elsevier BV

Subject

Cell Biology,Endocrinology,Biochemistry

Reference46 articles.

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4. Abetalipoproteinemia is caused by defects of the gene encoding the 97 kDa subunit of a microsomal triglyceride transfer protein;Shoulders;Hum. Mol. Genet.,1993

5. The role of the microsomal triglygeride transfer protein in abetalipoproteinemia;Berriot-Varoqueaux;Annu. Rev. Nutr.,2000

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