The Genetic Programs Behind Cerebellar Development
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Publisher
Springer International Publishing
Link
https://link.springer.com/content/pdf/10.1007/978-3-031-15070-8_20
Reference54 articles.
1. Aldinger KA, Doherty D (2016) The genetics of cerebellar malformations. Semin Fetal Neonatal Med 21:321–332
2. Aldinger KA, Lehmann OJ, Hudgins L, Chizhikov VV, Bassuk AG, Ades LC, Krantz ID, Dobyns WB, Millen KJ (2009) FOXC1 is required for normal cerebellar development and is a major contributor to chromosome 6p25.3 Dandy–Walker malformation. Nat Genet 41:1037–1042
3. Aldinger KA, Mendelsohn NJ, Chung BH, Zhang W, Cohn DH, Fernandez B, Alkuraya FS, Dobyns WB, Curry CJ (2016) Variable brain phenotype primarily affects the brainstem and cerebellum in patients with osteogenesis imperfecta caused by recessive WNT1 mutations. J Med Genet 53:427–430
4. Aldinger KA, Timms AE, Thomson Z, Mirzaa GM, Bennett JT, Rosenberg AB, Roco CM, Hirano M, Abidi F, Haldipur P et al (2019) Redefining the etiologic landscape of cerebellar malformations. Am J Hum Genet 105:606–615
5. Aldinger KA, Thomson Z, Phelps IG, Haldipur P, Deng M, Timms AE, Hirano M, Santpere G, Roco C, Rosenberg AB et al (2021) Spatial and cell type transcriptional landscape of human cerebellar development. Nat Neurosci 24:1163–1175. https://doi.org/10.1038/s41593-021-00872-y
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