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Identification of genetic variants associated with skeletal muscle function deficit in childhood acute lymphoblastic leukemia survivors
Background: Although 80% of childhood acute lymphoblastic leukemia (ALL) cases are cured with current treatment protocols, exposure to chemotherapeutics or radiation therapy during a vulnerable period of child development has been associated with a high frequency of late adverse effects (LAE). Previ...
Autores principales: | Nadeau, Geneviève, Ouimet-Grennan, Erika, Aaron, Michelle, Drouin, Simon, Bertout, Laurence, Shalmiev, Albert, Beaulieu, Patrick, St-Onge, Pascal, Veilleux, Louis-Nicolas, Rauch, Frank, Petrykey, Kateryna, Laverdière, Caroline, Sinnett, Daniel, Alos, Nathalie, Krajinovic, Maja |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6489684/ https://www.ncbi.nlm.nih.gov/pubmed/31114288 http://dx.doi.org/10.2147/PGPM.S192924 |
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