A homozygous missense variant in UBE2T is associated with a mild Fanconi anemia phenotype

Detalles Bibliográficos
Autores principales: Schultz-Rogers, Laura, Lach, Francis P., Rickman, Kimberly A., Ferrer, Alejandro, Mangaonkar, Abhishek A., Schwab, Tanya L., Schmitz, Christopher T., Clark, Karl J., Dsouza, Nikita R., Zimmermann, Michael T., Litzow, Mark, Jacobi, Nicole, Klee, Eric W., Smogorzewska, Agata, Patnaik, Mrinal M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Fondazione Ferrata Storti 2021
Materias:
Letters to the Editor
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8018101/
https://www.ncbi.nlm.nih.gov/pubmed/32646888
http://dx.doi.org/10.3324/haematol.2020.259275

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8018101/
https://www.ncbi.nlm.nih.gov/pubmed/32646888
http://dx.doi.org/10.3324/haematol.2020.259275

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