DGAT1 mutation is linked to a congenital diarrheal disorder-Reference-Cited by-同舟云学术

DGAT1 mutation is linked to a congenital diarrheal disorder

Published:2012-11-01 Issue:12 Volume:122 Page:4680-4684
ISSN:0021-9738
Container-title:Journal of Clinical Investigation
language:en
Short-container-title:J. Clin. Invest.

Author:

Haas Joel T.,Winter Harland S.,Lim Elaine,Kirby Andrew,Blumenstiel Brendan,DeFelice Matthew,Gabriel Stacey,Jalas Chaim,Branski David,Grueter Carrie A.,Toporovski Mauro S.,Walther Tobias C.,Daly Mark J.,Farese Robert V.

Publisher

American Society for Clinical Investigation

Subject

General Medicine

Reference26 articles.

1. Congenital Diarrheal Disorders: An Updated Diagnostic Approach

2. Congenital Diarrheal Disorders: Improved Understanding of Gene Defects Is Leading to Advances in Intestinal Physiology and Clinical Management

3. Thematic Review Series: Glycerolipids. DGAT enzymes and triacylglycerol biosynthesis

4. Identification of a gene encoding an acyl CoA:diacylglycerol acyltransferase, a key enzyme in triacylglycerol synthesis

5. DGAT1 Is Not Essential for Intestinal Triacylglycerol Absorption or Chylomicron Synthesis

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