Molecular analysis and intestinal expression of <it>SAR1 </it>genes and proteins in Anderson's disease (Chylomicron retention disease)

<p>Abstract</p> <p>Background</p> <p>Anderson's disease (AD) or chylomicron retention disease (CMRD) is a very rare hereditary lipid malabsorption syndrome. In order to discover novel mutations in the <it>SAR1B </it>gene and to evaluate the expression,...

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Bibliographic Details
Main Authors: Boileau Catherine, Bruckert Eric, Guenedet Jean C, Aparicio Thomas, Abifadel Marianne, Rabès Jean P, Champigneulle Jacqueline, Bonnefont-Rousselot Dominique, Bonneau Jessica, Georges Amandine, Morali Alain, Varret Mathilde, Aggerbeck Lawrence P, Samson-Bouma Marie E
Format: Article
Language:English
Published: BMC 2011-01-01
Series:Orphanet Journal of Rare Diseases
Online Access:http://www.ojrd.com/content/6/1/1