Associated Papers
Characterization of the disease-causing mechanism of KIF3B mutations from ciliopathy patients.
Adams JM et al.
Frontiers in Molecular Biosciences, 2024
Development and validation of animal variant classification guidelines to objectively evaluate genetic variant pathogenicity in domestic animals.
Boeykens F et al.
Frontiers in Veterinary Science, 2024
39703406 (PubMed )
Supplement: Table_1.XLSX › Sheet1
KIF3B gene silent variant leading to sperm morphology and motility defects and male infertility†.
Heydari R et al.
Biology of Reproduction, 2022
A domestic cat whole exome sequencing resource for trait discovery.
Rodney AR et al.
Scientific Reports, 2021
33785770 (PubMed )
Supplement: 41598_2021_86200_MOESM6_ESM.xlsx › 99LivesExome41_2020__1000bp_-_K
Mutations in the Kinesin-2 Motor KIF3B Cause an Autosomal-Dominant Ciliopathy.
Cogné B et al.
American Journal of Human Genetics, 2020
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