Correcting the aberrant Fanconi anemia transcriptional program by gene therapy.

Dror, Yigal

Dror, Yigal.

Affiliation

Dror Y; Genetics and Genome Biology, Research Institute, The Hospital for Sick Children, Toronto, Ontario; Institute of Medical Science, Faculty of Medicine, University of Toronto; Division of Haematology/Oncology, Department of Paediatrics, The Hospital for Sick Children and University of Toronto, Ontario. yigal.dror@sickkids.ca.

Haematologica ; 108(10): 2566-2567, 2023 10 01.

Article in En | MEDLINE | ID: mdl-37288500

Subject(s)

Fanconi Anemia; Humans; Fanconi Anemia/genetics; Fanconi Anemia/therapy; Fanconi Anemia Complementation Group Proteins/genetics; Nuclear Proteins/genetics; Genetic Therapy; Fanconi Anemia Complementation Group A Protein/genetics

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Fanconi Anemia Limits: Humans Language: En Journal: Haematologica Year: 2023 Document type: Article Country of publication: Italy

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