Identification of novel mutations in BCKDHB and DBT genes in Vietnamese patients with maple sirup urine disease-Reference-Cited by-同舟云学术

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Identification of novel mutations in BCKDHB and DBT genes in Vietnamese patients with maple sirup urine disease

Published:2020-06-09 Issue:8 Volume:8 Page:
ISSN:2324-9269
Container-title:Molecular Genetics & Genomic Medicine
language:en
Short-container-title:Mol Genet Genomic Med

Author:

Nguyen Thi T. N.¹,Vu Chi D.²,Nguyen Ngoc L.¹³,Nguyen Thi T. H.¹³,Nguyen Ngoc K.²,Nguyen Huy H.¹^ORCID

Affiliation:

1. Institute of Genome ResearchVietnam Academy of Science and Technology (VAST) Hanoi Vietnam

2. National Hospital of Pediatrics Hanoi Vietnam

3. Graduate University of Science and TechnologyVietnam Academy of Science and Technology (VAST) Hanoi Vietnam

Funder

Vietnam Academy of Science and Technology

Publisher

Wiley

Subject

Genetics (clinical),Genetics,Molecular Biology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mgg3.1337

Reference30 articles.

1. In silico analysis of novel mutations in maple syrup urine disease patients from Iran

2. Fourteen new mutations of BCKDHA, BCKDHB and DBT genes associated with maple syrup urine disease (MSUD) in Malaysian population

3. Crystal structure of human branched-chain α-ketoacid dehydrogenase and the molecular basis of multienzyme complex deficiency in maple syrup urine disease

4. Maple syrup urine disease in five hereford calves in Ontario;Baird J. D.;Canadian Veterinary Journal,1987

5. Solution Structure and Dynamics of the Lipoic Acid-bearing Domain of Human Mitochondrial Branched-chain α-Keto Acid Dehydrogenase Complex

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Identification of gene mutations in six Chinese patients with maple syrup urine disease;Frontiers in Genetics;2023-02-24

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