Further delineation of putative ACTB loss‐of‐function variants: A 4‐patient series

ACTB encodes β‐cytoplasmic actin, an essential component of the cytoskeleton. Based on chromosome 7p22.1 deletions that include the ACTB locus and on rare truncating ACTB variants, a phenotype resulting from ACTB haploinsufficiency was recently proposed. We report putative ACTB loss‐of‐function vari...

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Detalles Bibliográficos
Autores principales: Baumann, Matthias, Beaver, Erin M., Palomares‐Bralo, María, Santos‐Simarro, Fernando, Holzer, Peter, Povysil, Gundula, Müller, Thomas, Valovka, Taras, Janecke, Andreas R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Brief Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7155001/
https://www.ncbi.nlm.nih.gov/pubmed/31898838
http://dx.doi.org/10.1002/humu.23970

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7155001/
https://www.ncbi.nlm.nih.gov/pubmed/31898838
http://dx.doi.org/10.1002/humu.23970

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