Infantile type of homocystinuria with N5,10-methylenetetrahydrofolate reductase defect.-Reference-Cited by-同舟云学术

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Infantile type of homocystinuria with N5,10-methylenetetrahydrofolate reductase defect.

Published:1977 Issue:2 Volume:121 Page:185-194
ISSN:0040-8727
Container-title:The Tohoku Journal of Experimental Medicine
language:en
Short-container-title:Tohoku J. Exp. Med.

Author:

NARISAWA KUNIAKI¹,WADA YOSHIRO¹,SAITO TAKASHI¹,SUZUIKI HIROSHI¹,KUDO MASAFUMI¹,ARAKAWA TSUNEO¹,KATSUSHIMA NORIKO¹²,TSUBOI REIKO¹²

Affiliation:

1. Department of Pediatrics, Tohoku University School of Medicine

2. Pediatric Clinic, Yamagata City Hospital

Publisher

Tohoku University Medical Press

Subject

General Biochemistry, Genetics and Molecular Biology,General Medicine

Link

http://www.jstage.jst.go.jp/article/tjem1920/121/2/121_2_185/_pdf

Cited by 29 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. Prenatal Diagnosis of Miscellaneous Biochemical Disorders;Genetic Disorders and the Fetus;2015-11-23

2. Reversal of Respiratory Failure in Both Neonatal and Late Onset Isolated Remethylation Disorders;JIMD Reports;2014

3. Prenatal Diagnosis of Miscellaneous Biochemical Disorders;Genetic Disorders and the Fetus;2010-09-24

4. Severe Methylenetetrahydrofolate Reductase (MTHFR) Deficiency: A Case Report of Nonclassical Homocystinuria;Journal of Child Neurology;2008-07

5. Diseases of Sulphur Metabolism: Implications for the Methionine-Homocysteine Cycle, and Vitamin Responsiveness;Ciba Foundation Symposium 72 - Sulphur in Biology;2008-05-30

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