Cargando…
P754: PRIME EDITING AS A NOVEL TOOL FOR PRECISE CORRECTION OF CAUSAL MUTATIONS IN FANCONI ANAEMIA GROUP A PATIENT-DERIVED CELLS
Autores principales: | Peterkova, Lucie, Racková, Markéta, Svaton, Michael, Riha, Petr, Novotna, Drahuse, Sedlacek, Petr, Sramkova, Lucie, Skvarova, Karolina |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10429436/ http://dx.doi.org/10.1097/01.HS9.0000969920.27248.b5 |
Ejemplares similares
-
Novel SAMD9 Mutation in a Patient With Immunodeficiency, Neutropenia, Impaired Anti-CMV Response, and Severe Gastrointestinal Involvement
por: Formankova, Renata, et al.
Publicado: (2019) -
A 15 Mb large paracentric chromosome 21 inversion identified in Czech population through a pair of flanking duplications
por: Drabova, Jana, et al.
Publicado: (2014) -
Understanding complexity of Fanconi anaemia
por: Mohanty, Dipika
Publicado: (2016) -
Fanconi's anaemia & Laron syndrome: An enigma
por: Kashyap, Rajesh, et al.
Publicado: (2020) -
754 Improving antibiotic delivery in the ICU
por: Lakshmi, Seetha, et al.
Publicado: (2014)