An ovine hepatorenal fibrocystic model of a Meckel-like syndrome associated with dysmorphic primary cilia and TMEM67 mutations. [electronic resource]
Producer: 20181211Description: 1601 p. digitalISSN:- 2045-2322
- Abnormalities, Multiple -- genetics
- Amino Acid Substitution
- Animals
- Base Sequence
- Chromosomes, Mammalian -- genetics
- Cilia -- pathology
- Dandy-Walker Syndrome -- genetics
- Disease Models, Animal
- Epithelial Cells -- metabolism
- Genetic Loci
- Golgi Apparatus -- metabolism
- Hepatorenal Syndrome -- genetics
- Homozygote
- Kidney -- pathology
- Membrane Proteins -- chemistry
- Mutation -- genetics
- Mutation, Missense -- genetics
- Pancreatic Cyst -- genetics
- RNA, Messenger -- genetics
- Sheep
- Zebrafish
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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