Loss of CBY1 results in a ciliopathy characterized by features of Joubert syndrome is a research paper published in Human Mutation (2020). On theSindex it has a DataRank of 0. It has been cited 21 times.
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Deutsche Forschungsgemeinschaft
Grant: BE 3910/8‐1
Deutsche Forschungsgemeinschaft
Grant: BE 3910/9‐1
National Institute of Child Health and Human Development
Grant: U54HG006493
NICHD NIH HHS
Grant: P50 HD103524
NIGMS NIH HHS
Grant: R01 GM121317
NICHD NIH HHS
Grant: R01 HD100730
NICHD NIH HHS
Grant: R01 HD042601
NIDDK NIH HHS
Grant: R01 DK072301
NINDS NIH HHS
Grant: R01 NS064077
European Research Council
Grant: 716344
Novel Therapeutic Avenues for dynein-related Ciliopathies
NHGRI NIH HHS
Grant: UM1 HG006493
National Institutes of Health
Grant: 5R01HD042601-02
Molecular Genetics of Bardet-Biedl Syndrome
National Institutes of Health
Grant: 5R01GM121317-12
The Role of Basal Bodies in Wnt Signaling
Deutsche Forschungsgemeinschaft
Grant: unidentified
unidentified
National Institutes of Health
Grant: 1U54HG006493-01
UW Center for Mendelian Genomics
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