标题:Clinical features and ETFDH mutation spectrum in a cohort of 90 chinese patients with late-onset multiple acyl-CoA dehydrogenase deficiency
作者:Xi,J.;Wen,B.;Lin,J.;Zhu,W.;Luo,S.;Zhao,C.;Li,D.;Lin,P.;Lu,J.;Yan,C.
作者机构:[Xi, J] Department of Neurology, Huashan Hospital, Fudan University, Shanghai 200040, China, Institute of Neurology, Huashan Hospital, Fudan Universit 更多
通讯作者:Lu, JH
通讯作者地址:[Lu, JH]Fudan Univ, Huashan Hosp, Dept Neurol, Shanghai 200040, Peoples R China.
来源:Journal of inherited metabolic disease
出版年:2014
卷:37
期:3
页码:399-404
DOI:10.1007/s10545-013-9671-6
摘要:The major cause of lipid storagemyopathies (LSM) in China is multiple acyl-CoA dehydrogenase deficiency (MADD) caused by ETFDH mutations. We here present an analysis of the spectrum of ETFDH mutations in the largest cohort of patients with MADD (90 unrelated patients). We identified 61 ETFDH mutations, including 31 novel mutations, which were widely distributed within the coding sequence. Three frequent mutations were identified: c.250G>A (most common in South China), c.770A>G and c.1227A>C (most common in both South and North China). Regional differences of allele frequency and further haplotype analysis suggest the possibility of founder effects of c.250G>A and c.770A>G. These findings promise to provide the basis for implementing a rapid and economical strategy for diagnosing MADD.
收录类别:SCOPUS;SCIE
WOS核心被引频次:13
Scopus被引频次:17
资源类型:期刊论文
原文链接:https://www.scopus.com/inward/record.uri?eid=2-s2.0-84904179705&doi=10.1007%2fs10545-013-9671-6&partnerID=40&md5=bea39654c61708b0668586e1b6cb8b52
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