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Bi-allelic CAMSAP1 variants cause a clinically recognizable neuronal migration disorder.
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Bi-allelic CAMSAP1 variants cause a clinically recognizable neuronal migration disorder.
Bi-allelic CAMSAP1 variants cause a clinically recognizable neuronal migration disorder. Am J Hum Genet. 2022 11 03; 109(11):2068-2079.
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PubMed
subject areas
Alleles
Animals
Classical Lissencephalies and Subcortical Band Heterotopias
Humans
Lissencephaly
Mice
Mice, Knockout
Microtubule-Associated Proteins
Nervous System Malformations
Phenotype
Tubulin
authors with profiles
William B. Dobyns