Liver Disease and Risk of Hepatocellular Carcinoma in Children With Mutations in TALDO1-Reference-Cited by-同舟云学术

Liver Disease and Risk of Hepatocellular Carcinoma in Children With Mutations in TALDO1

Published:2021-10-22 Issue: Volume: Page:
ISSN:2471-254X
Container-title:Hepatology Communications
language:en
Short-container-title:Hepatol Commun

Author:

Grammatikopoulos Tassos¹²^ORCID,Hadzic Nedim¹,Foskett Pierre³,Strautnieks Sandra³,Samyn Marianne¹,Vara Roshni⁴,Dhawan Anil¹,Hertecant Jozef⁵,Al Jasmi Fatma⁵,Rahman Obydur³,Deheragoda Maesha³,Bull Laura N.⁶,Thompson Richard J¹²,

Affiliation:

1. Pediatric Liver, GI & Nutrition Center and MowatLabs King’s College Hospital London United Kingdom

2. Institute of Liver Studies King’s College London London United Kingdom

3. Institute of Liver Studies King’s College Hospital London United Kingdom

4. Department of Pediatric Inherited Metabolic Diseases Evelina Children’s Hospital London United Kingdom

5. Division of Genetics/Metabolics Department of Pediatrics Tawam Hospital Al Ain United Arab Emirates

6. Institute for Human Genetics and Liver Center Laboratory Department of Medicine University of California San Francisco San Francisco CA USA

Funder

National Heart, Lung, and Blood Institute

Foundation for the National Institutes of Health

National Human Genome Research Institute

Publisher

Wiley

Subject

General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/hep4.1824

Reference17 articles.

1. Transaldolase Deficiency: Liver Cirrhosis Associated with a New Inborn Error in the Pentose Phosphate Pathway

2. Systemic lupus erythematosus in a girl with PTEN variant and transaldolase deficiency: a novel phenotype

3. Hypergonadotrophic hypogonadism in a patient with transaldolase deficiency: novel mutation in the pentose phosphate pathway

4. Clinical, biochemical, and molecular overview of transaldolase deficiency and evaluation of the endocrine function: Update of 34 patients

5. Transaldolase deficiency: A new cause of hydrops fetalis and neonatal multi-organ disease

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