Novel Jbts17 mutant mouse model of Joubert syndrome with cilia transition zone defects and cerebellar and other ciliopathy related anomalies.
Hum Mol Genet
; 24(14): 3994-4005, 2015 Jul 15.
Article
in En
| MEDLINE
| ID: mdl-25877302
Full text:
1
Database:
MEDLINE
Main subject:
Retina
/
Cerebellar Diseases
/
Cerebellum
/
Membrane Proteins
Type of study:
Prognostic_studies
Language:
En
Year:
2015
Type:
Article