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,...
Main Authors: | , , , , , , , , , , , , , |
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Format: | Article |
Language: | English |
Published: |
BMC
2011-01-01
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Series: | Orphanet Journal of Rare Diseases |
Online Access: | http://www.ojrd.com/content/6/1/1 |