Van Der Werf, Christine S <br/><br/>
CLMP is required for intestinal development, and loss-of-function mutations cause congenital short-bowel syndrome.  [electronic resource] 

 -  Gastroenterology  Mar 2012 
 - 453-462.e3 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1528-0012 
<br/><br/><label>Standard No.: </label>10.1053/j.gastro.2011.11.038  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Animals<br/>CHO Cells<br/>Child<br/>Child, Preschool<br/>Coxsackie and Adenovirus Receptor-Like Membrane Protein<br/>Cricetinae<br/>Cricetulus<br/>Disease Models, Animal<br/>Female<br/>Gene Expression Regulation, Developmental<br/>Genetic Predisposition to Disease<br/>Heterozygote<br/>Homozygote<br/>Humans<br/>Infant<br/>Infant, Newborn<br/>Intestine, Small--abnormalities<br/>Male<br/>Morphogenesis<br/>Mutation, Missense<br/>Phenotype<br/>Polymorphism, Single Nucleotide<br/>Receptors, Virus--genetics<br/>Short Bowel Syndrome--embryology<br/>Transfection<br/>Young Adult<br/>Zebrafish--embryology<br/>Zebrafish Proteins--genetics