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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

Crossref DOI link: https://doi.org/10.1007/s11033-022-08071-z

Published Online: 2022-11-11

Published Print: 2023-01

Update policy: https://doi.org/10.1007/springer_crossmark_policy

Authors

Behera, Chinmay Kumar

Gyandeep, Gummalla

Mishra, Reshmi

Mohanty, Rashmi Priya

Pal, Aditi

Behera, Jyotika

Samal, Sagnika

Das, Biswadeep https://orcid.org/0000-0001-8214-3600
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Article History

Received: 9 August 2022

Accepted: 31 October 2022

First Online: 11 November 2022

Declarations

:

: The authors have no relevant financial or non-financial interests to disclose.

: This study was performed and approved by the Institute Ethical Committee of KIIT School of Biotechnology, KIIT University, Bhubaneswar.

: Written informed consent was obtained from the parents.

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