Generation of four H1 hESC sublines carrying a hemizygous knock-out/mutant MECP2
Rett syndrome (RTT) is a childhood neurodevelopmental disorder caused by mutations in MECP2. To study the molecular mechanisms underlying RTT, four sublines of H1 hESCs were generated, carrying a hemizygous knockout or mutant allele of MECP2. Exons 3 and 4 of MECP2 were targeted using the CRISPR/Cas...
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| Autores principales: | , , , , , |
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| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
Elsevier
2019-10-01
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| Colección: | Stem Cell Research |
| Acceso en línea: | http://www.sciencedirect.com/science/article/pii/S1873506119301631 |
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