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AHI1 mutations cause both retinal dystrophy and renal cystic disease in Joubert syndrome.
Consensus Paper: Cerebellar Development.
RTTN mutations link primary cilia function to organization of the human cerebral cortex.
Wnt coreceptor Lrp5 is a driver of idiopathic pulmonary fibrosis.
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Consensus Paper: Cerebellar Development.
Consensus Paper: Cerebellar Development. Cerebellum. 2016 12; 15(6):789-828.
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PubMed
subject areas
Animals
Cerebellum
Consensus
Humans
Neurogenesis
Neurons
authors with profiles
William B. Dobyns