Result: Loss of CBY1 results in a ciliopathy characterized by features of Joubert syndrome

*Title*:

*Author/editor-in-chief*:

*Publication*:

Freiburg : Universität, 2020

*Physical description scale*:

Online-Ressource

*Format*:

*eBook*

*Language*:

*eng*

*Notes*:

Human mutation
41, 12 (2020) , 2179-2194, ISSN: 1098-1004

*DOI*:

10.1002/humu.24127

*Result*: Loss of CBY1 results in a ciliopathy characterized by features of Joubert syndrome