Role of Nesprin-2 and RanBP2 in BICD2-associated brain developmental disorders

Bicaudal D2 (BICD2) is responsible for recruiting cytoplasmic dynein to diverse forms of subcellular cargo for their intracellular transport. Mutations in the human BICD2 gene have been found to cause an autosomal dominant form of spinal muscular atrophy (SMA-LED2), and brain developmental defects....

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Detalles Bibliográficos
Autores principales: Yi, Julie, Zhao, Xiaoxin, Noell, Crystal R., Helmer, Paige, Solmaz, Sozanne R., Vallee, Richard B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2023
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10022797/
https://www.ncbi.nlm.nih.gov/pubmed/36930595
http://dx.doi.org/10.1371/journal.pgen.1010642

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10022797/
https://www.ncbi.nlm.nih.gov/pubmed/36930595
http://dx.doi.org/10.1371/journal.pgen.1010642

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