TY  - GEN
AU  - Stayner,C
AU  - Poole,C A
AU  - McGlashan,S R
AU  - Pilanthananond,M
AU  - Brauning,R
AU  - Markie,D
AU  - Lett,B
AU  - Slobbe,L
AU  - Chae,A
AU  - Johnstone,A C
AU  - Jensen,C G
AU  - McEwan,J C
AU  - Dittmer,K
AU  - Parker,K
AU  - Wiles,A
AU  - Blackburne,W
AU  - Leichter,A
AU  - Leask,M
AU  - Pinnapureddy,A
AU  - Jennings,M
AU  - Horsfield,J A
AU  - Walker,R J
AU  - Eccles,M R
TI  - An ovine hepatorenal fibrocystic model of a Meckel-like syndrome associated with dysmorphic primary cilia and TMEM67 mutations
SN  - 2045-2322
PY  - 2018///1211
KW  - Abnormalities, Multiple
KW  - genetics
KW  - Amino Acid Substitution
KW  - Animals
KW  - Base Sequence
KW  - Chromosomes, Mammalian
KW  - Cilia
KW  - pathology
KW  - Dandy-Walker Syndrome
KW  - Disease Models, Animal
KW  - Epithelial Cells
KW  - metabolism
KW  - Genetic Loci
KW  - Golgi Apparatus
KW  - Hepatorenal Syndrome
KW  - Homozygote
KW  - Kidney
KW  - Membrane Proteins
KW  - chemistry
KW  - Mutation
KW  - Mutation, Missense
KW  - Pancreatic Cyst
KW  - RNA, Messenger
KW  - Sheep
KW  - Zebrafish
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1038/s41598-017-01519-4
ER  -