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Using CRISPR/Cas9 genome editing in human iPSCs for deciphering the pathogenicity of a novel CCM1 transcription start site deletion
Cerebral cavernous malformations are clusters of aberrant vessels that can lead to severe neurological complications. Pathogenic loss-of-function variants in the CCM1, CCM2, or CCM3 gene are associated with the autosomal dominant form of the disease. While interpretation of variants in protein-codin...
Autores principales: | Pilz, Robin A., Skowronek, Dariush, Hamed, Motaz, Weise, Anja, Mangold, Elisabeth, Radbruch, Alexander, Pietsch, Torsten, Felbor, Ute, Rath, Matthias |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9453596/ https://www.ncbi.nlm.nih.gov/pubmed/36090026 http://dx.doi.org/10.3389/fmolb.2022.953048 |
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