Incidence of medium-chain acyl-CoA dehydrogenase deficiency in Canada using the Canadian Paediatric Surveillance Program: Role of newborn screening-Reference-Cited by-同舟云学术

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Incidence of medium-chain acyl-CoA dehydrogenase deficiency in Canada using the Canadian Paediatric Surveillance Program: Role of newborn screening

Published:2012-04-01 Issue:4 Volume:17 Page:185-189
ISSN:1205-7088
Container-title:Paediatrics & Child Health
language:en
Short-container-title:

Author:

Prasad Chitra,Speechley Kathy N,Dyack Sarah,Rupar Charles A,Chakraborty Pranesh,Kronick Jonathan B

Publisher

Oxford University Press (OUP)

Subject

Pediatrics, Perinatology and Child Health

Link

http://academic.oup.com/pch/article-pdf/17/4/185/23628928/pch17185.pdf

Reference27 articles.

1. On line Mendelian Inheritance in Man OMIM (Accessed on September 1, 2011).

2. Morbidity and mortality in medium chain acyl coenzyme A dehydrogenase deficiency;Wilcken;Arch Dis Child,1994

3. Population spectrum of ACADM genotypes correlated to biochemical phenotypes in newborn screening for medium-chain acyl-CoA dehydrogenase deficiency;Maier;Hum Mutat,2005

4. Newborn screening for medium-chain acyl-CoA dehydrogenase deficiency: A global perspective;Rhead;J Inherit Metab Dis,2006

5. Fatty acid oxidation defects as causes of unexpected death in infancy;Bennett;Prog Clin Biol Res,1990

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. Screening of MCAD deficiency in Japan: 16years' experience of enzymatic and genetic evaluation;Molecular Genetics and Metabolism;2016-12

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