Specific correction of pyruvate kinase deficiency-causing point mutations by CRISPR/Cas9 and single-stranded oligodeoxynucleotides

Pyruvate kinase deficiency (PKD) is an autosomal recessive disorder caused by mutations in the PKLR gene. PKD-erythroid cells suffer from an energy imbalance caused by a reduction of erythroid pyruvate kinase (RPK) enzyme activity. PKD is associated with reticulocytosis, splenomegaly and iron overlo...

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Detalles Bibliográficos
Autores principales: Fañanas-Baquero, Sara, Morín, Matías, Fernández, Sergio, Ojeda-Perez, Isabel, Dessy-Rodriguez, Mercedes, Giurgiu, Miruna, Bueren, Juan A., Moreno-Pelayo, Miguel Angel, Segovia, Jose Carlos, Quintana-Bustamante, Oscar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Genome Editing
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10175809/
https://www.ncbi.nlm.nih.gov/pubmed/37188156
http://dx.doi.org/10.3389/fgeed.2023.1104666

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10175809/
https://www.ncbi.nlm.nih.gov/pubmed/37188156
http://dx.doi.org/10.3389/fgeed.2023.1104666

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