Author:
Beijer Danique,Züchner Stephan L.
Subject
Cellular and Molecular Neuroscience,Molecular Biology
Reference12 articles.
1. Nonsense mutations in alpha-II spectrin in three families with juvenile onset hereditary motor neuropathy;Beijer;Brain,2019
2. Spectrin mutations cause spinocerebellar ataxia type 5;Ikeda;Nat. Genet.,2006
3. SPTBN5, encoding the betaV-spectrin protein, leads to a syndrome of intellectual disability, developmental delay, and seizures;Khan;Front. Mol. Neurosci.,2022
4. A recessive mutation in beta-IV-spectrin (SPTBN4) associates with congenital myopathy, neuropathy, and central deafness;Knierim;Hum. Genet.,2017
5. Recessive mutations in SPTBN2 implicate beta-III spectrin in both cognitive and motor development;Lise;PLoS Genet.,2012
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