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Identification of Compounds That Promote Readthrough of Premature Termination Codons in the CFTR
Cystic fibrosis (CF) is caused by a mutation of the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) gene, which disrupts an ion channel involved in hydration maintenance via anion homeostasis. Nearly 5% of CF patients possess one or more copies of the G542X allele, which results in a stop...
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| Publicado no: | SLAS Discov |
|---|---|
| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
SAGE Publications
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7838340/ https://ncbi.nlm.nih.gov/pubmed/33016182 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/2472555220962001 |
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