A Rare Case of Pediatric Hepatocellular Carcinoma Secondary to Mitochondrial DNA Depletion Syndrome Type 3 ( <i>DGUOK</i> Mutation)

Authors

Arjun Maria
Shaleen Agarwal (ORCID: https://orcid.org/0000-0002-5187-7799)
Saphalta Baghmar (ORCID: https://orcid.org/0000-0002-7713-3851)
Gaurav Khanna (ORCID: https://orcid.org/0000-0001-9129-3686)
Prashant Mehta (ORCID: https://orcid.org/0000-0002-8151-4331)
Vidit Kapoor
Pravas Mishra
Moushumi Suryavanshi
Tejasvi R

Institutions

Amrita Vishwa Vidyapeetham (IN)

Publication Details

Journal: Pediatric Blood & Cancer
Published: 2026-03-15
DOI: https://doi.org/10.1002/1545-5017.70220
Primary Topic: Mitochondrial Function and Pathology
Type: article
Field-Weighted Citation Impact: 0.00

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article

A Rare Case of Pediatric Hepatocellular Carcinoma Secondary to Mitochondrial DNA Depletion Syndrome Type 3 ( DGUOK Mutation)

Arjun Maria, Shaleen Agarwal, Saphalta Baghmar, Gaurav Khanna et al.

Mar 15, 2026

Pediatric Blood & Cancer

Mitochondrial Function and Pathology

article

A Rare Case of Pediatric Hepatocellular Carcinoma Secondary to Mitochondrial DNA Depletion Syndrome Type 3 ( DGUOK Mutation)

Arjun Maria, Shaleen Agarwal, Saphalta Baghmar, Gaurav Khanna, Prashant Mehta, Vidit Kapoor, Pravas Mishra, Moushumi Suryavanshi, Tejasvi R

March 15, 2026article en

Abstract

No abstract available for this paper.

Pediatric Blood & Cancer

Amrita Vishwa Vidyapeetham (IN)

Openalex Percentile: Top 20%

Mitochondrial Function and Pathology

DOI Source OpenAlex

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