Detection of a novel SNX2 gene breakpoint in the SNX2::ABL1 fusion transcript in Ph‐like B‐cell acute lymphoblastic leukemia-Reference-Cited by-同舟云学术

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Detection of a novel SNX2 gene breakpoint in the SNX2::ABL1 fusion transcript in Ph‐like B‐cell acute lymphoblastic leukemia

Published:2023-07-06 Issue:10 Volume:70 Page:
ISSN:1545-5009
Container-title:Pediatric Blood & Cancer
language:en
Short-container-title:Pediatric Blood & Cancer

Author:

Leons Gadha K.¹,Sharma Preity¹,Gupta Sanjeev Kumar¹^ORCID,Gupta Ritu¹,Rani Lata²,Gajendra Smeeta¹,Roy Anita³,Sahoo Ranjit Kumar⁴

Affiliation:

1. Laboratory Oncology Unit Dr BRA IRCH All India Institute of Medical Sciences New Delhi India

2. Centralized Core Research Facility Genomics Facility All India Institute of Medical Sciences New Delhi India

3. Kusuma School of Biological Sciences Indian Institute of Technology New Delhi India

4. Department of Medical Oncology Dr BRA IRCH All India Institute of Medical Sciences New Delhi India

Funder

Indian Council of Medical Research

Publisher

Wiley

Subject

Oncology,Hematology,Pediatrics, Perinatology and Child Health

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/pbc.30546

Reference19 articles.

1. Molecular genetics of B-precursor acute lymphoblastic leukemia

2. Deletion ofIKZF1and Prognosis in Acute Lymphoblastic Leukemia

3. KamranS RacaG NazirK.RCSD1‐ABL1 translocation associated with IKZF1 gene deletion in B‐cell acute lymphoblastic leukemia.Case Rep Hematol.2015;2015:353247. doi:10.1155/2015/353247

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