Stayner, C <br/><br/>
An ovine hepatorenal fibrocystic model of a Meckel-like syndrome associated with dysmorphic primary cilia and TMEM67 mutations.  [electronic resource] 

 -  Scientific reports  05 2017 
 - 1601 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>2045-2322 
<br/><br/><label>Standard No.: </label>10.1038/s41598-017-01519-4  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--genetics<br/>Amino Acid Substitution<br/>Animals<br/>Base Sequence<br/>Chromosomes, Mammalian--genetics<br/>Cilia--pathology<br/>Dandy-Walker Syndrome--genetics<br/>Disease Models, Animal<br/>Epithelial Cells--metabolism<br/>Genetic Loci<br/>Golgi Apparatus--metabolism<br/>Hepatorenal Syndrome--genetics<br/>Homozygote<br/>Kidney--pathology<br/>Membrane Proteins--chemistry<br/>Mutation--genetics<br/>Mutation, Missense--genetics<br/>Pancreatic Cyst--genetics<br/>RNA, Messenger--genetics<br/>Sheep<br/>Zebrafish