Establishment of human embryonic stem cell lines carrying LQT1 mutations by CRISPR base editing
The KCNQ1 gene encodes a voltage-gated potassium channel required for cardiac action potentials. Mutations in this gene have been associated with hereditary long QT syndrome 1, Jervell and Lange-Nielsen syndromes, and familial atrial fibrillation. The NM_000218.3(KCNQ1): c.604 + 2T > C mutation has...
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| Autors principals: | , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Elsevier
2024-09-01
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| Col·lecció: | Stem Cell Research |
| Accés en línia: | http://www.sciencedirect.com/science/article/pii/S1873506124001946 |
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