Genetic analysis of a Fanconi anemia case revealed the presence of FANCF mutation (exon 1;469>C-T) with implications to develop acute myeloid leukemia-Reference-Cited by-同舟云学术

Genetic analysis of a Fanconi anemia case revealed the presence of FANCF mutation (exon 1;469>C-T) with implications to develop acute myeloid leukemia

Published:2022-11-11 Issue:1 Volume:50 Page:931-936
ISSN:0301-4851
Container-title:Molecular Biology Reports
language:en
Short-container-title:Mol Biol Rep

Author:

Behera Chinmay Kumar,Gyandeep Gummalla,Mishra Reshmi,Mohanty Rashmi Priya,Pal Aditi,Behera Jyotika,Samal Sagnika,Das Biswadeep^ORCID

Publisher

Springer Science and Business Media LLC

Subject

Genetics,Molecular Biology,General Medicine

Link

https://link.springer.com/content/pdf/10.1007/s11033-022-08071-z.pdf

Reference17 articles.

1. Moreno OM, Paredes AC, Suarez-Obando F, Rojas A (2021) An update on Fanconi anemia: clinical, cytogenetic and molecular approaches (review). Biomed Rep 15:1–10. https://doi.org/10.3892/BR.2021.1450/HTML

2. García-De-Teresa B, Rodríguez A, Frias S (2020) Chromosome instability in Fanconi Anemia: from breaks to phenotypic consequences. Genes (Basel). https://doi.org/10.3390/genes11121528

3. Bhandari J, Thada PK, Puckett Y (2022) Fanconi anemia. StatPearls

4. George M, Solanki A, Chavan N et al (2021) A comprehensive molecular study identified 12 complementation groups with 56 novel FANC gene variants in Indian Fanconi anemia subjects. Hum Mutat 42:1648–1665. https://doi.org/10.1002/HUMU.24286

5. Liu W, Palovcak A, Li F et al (2020) Fanconi anemia pathway as a prospective target for cancer intervention. Cell Biosci. https://doi.org/10.1186/s13578-020-00401-7

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