Medium‐chain acyl‐coenzyme A dehydrogenase deficiency: Six cases in the Chinese population-Reference-Cited by-同舟云学术

Medium‐chain acyl‐coenzyme A dehydrogenase deficiency: Six cases in the Chinese population

Published:2019-06-14 Issue: Volume: Page:
ISSN:1328-8067
Container-title:Pediatrics International
language:en
Short-container-title:Pediatrics International

Author:

Li Yanhan¹,Zhu Ruoxin²,Liu Yi³,Song Jinqing³,Xu Jing⁴,Yang Yanling³^ORCID

Affiliation:

1. Department of Laboratory Animal Center Institute of Hematology and Blood Diseases Hospital Chinese Academy of Medical Sciences and Peking Union Medical College TianjinChina

2. Department of Reproductive center Gansu Provincial Maternity and Child‐care Hospital Lanzhou, GansuChina

3. Department of Pediatrics Peking University First Hospital Beijing China

4. State Key Laboratory of Experimental Hematology Institute of Hematology and Blood Diseases Hospital Center for Stem Cell Medicine Chinese Academy of Medical Sciences and Peking Union Medical College TianjinChina

Publisher

Wiley

Subject

Pediatrics, Perinatology and Child Health

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/ped.13872

Reference40 articles.

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2. The epidemiology of medium chain acyl‐CoA dehydrogenase deficiency: An update;Grosse SD;Genet. Med.,2006

3. Screening of MCAD deficiency in Japan: 16 years’ experience of enzymatic and genetic evaluation;Tajima G;Mol. Genet. Metab.,2016

4. Neonatal screening for medium chain acyl‐CoA deficiency: High incidence in Lower Saxony (northern Germany);Sander S;Eur. J. Pediatr.,2001

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

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