CLMP is required for intestinal development, and loss-of-function mutations cause congenital short-bowel syndrome. [electronic resource]
Producer: 20120509Description: 453-462.e3 p. digitalISSN:- 1528-0012
- Adolescent
- Adult
- Animals
- CHO Cells
- Child
- Child, Preschool
- Coxsackie and Adenovirus Receptor-Like Membrane Protein
- Cricetinae
- Cricetulus
- Disease Models, Animal
- Female
- Gene Expression Regulation, Developmental
- Genetic Predisposition to Disease
- Heterozygote
- Homozygote
- Humans
- Infant
- Infant, Newborn
- Intestine, Small -- abnormalities
- Male
- Morphogenesis
- Mutation, Missense
- Phenotype
- Polymorphism, Single Nucleotide
- Receptors, Virus -- genetics
- Short Bowel Syndrome -- embryology
- Transfection
- Young Adult
- Zebrafish -- embryology
- Zebrafish Proteins -- genetics
No physical items for this record
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
There are no comments on this title.
Log in to your account to post a comment.