Associated Papers
Disease-associated mutations in WDR34 lead to diverse impacts on the assembly and function of dynein-2.
Shak C et al.
Journal of Cell Science, 2023
WDR34, a candidate gene for non-syndromic rod-cone dystrophy.
Solaguren-Beascoa M et al.
Clinical Genetics, 2021
Mutations in the gene encoding IFT dynein complex component WDR34 cause Jeune asphyxiating thoracic dystrophy.
Schmidts M et al.
American Journal of Human Genetics, 2013
Select a paper to view details