Homocystinuria in Taiwan: An inordinately high prevalence in an Austronesian aboriginal tribe, Tao-Reference-Cited by-同舟云学术

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Homocystinuria in Taiwan: An inordinately high prevalence in an Austronesian aboriginal tribe, Tao

Published:2012-04 Issue:4 Volume:105 Page:590-595
ISSN:1096-7192
Container-title:Molecular Genetics and Metabolism
language:en
Short-container-title:Molecular Genetics and Metabolism

Author:

Lu Yung-Hsiu,Huang Yu-Hsiu,Cheng Li-Mei,Yu Hsiao-Chi,Hsu Ju-Hui,Wu Tina Jui-Ting,Lo Ming-Yu,Lin Andrew,Lin Ching-Yuang,Wu Jer-Yuarn,Niu Dau-Ming

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference24 articles.

1. Disorders of transsulfuration;Mudd,2009

2. Newborn screening for homocystinuria: Irish and world experience;Naughten;Eur. J. Pediatr.,2000

3. Prevalence of congenital homocystinuria in Denmark;Gaustadnes;N. Engl. J. Med.,1999

4. Birth prevalence of homocystinuria;Refsum;J. Pediatr.,2004

5. High prevalence of the I278T mutation of the human cystathionine beta-synthase detected by a novel screening application;Linnebank;Thromb. Haemost.,2001

Cited by 9 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. Proteomic exploration of cystathionine β-synthase deficiency: implications for the clinic;Expert Review of Proteomics;2020-10-02

2. Classical homocystinuria: A common inborn error of metabolism? An epidemiological study based on genetic databases;Molecular Genetics & Genomic Medicine;2020-03-30

3. Sex affects N-homocysteinylation at lysine residue 212 of albumin in mice;Scientific Reports;2019-02-25

4. Three Main Causes of Homocystinuria: CBS, cblC and MTHFR Deficiency. What do they Have in Common?;Journal of Inborn Errors of Metabolism and Screening;2019

5. Heterozygous carriers of classical homocystinuria tend to have higher fasting serum homocysteine concentrations than non-carriers in the presence of folate deficiency;Clinical Nutrition;2015-12

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