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 mutation from anencephaly patients impaired both SHH and PCP signaling pathways.
Yin H et al.
Journal of Human Genetics, 2020
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
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