Literature DB >> 30128629

Multiple Acyl-CoA Dehydrogenase Deficiency in an Infant.

Xiao-Ming Hu1, Li Li2.   

Abstract

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Year:  2018        PMID： 30128629     DOI： 10.1007/s12098-018-2768-z

Source DB:  PubMed          Journal:  Indian J Pediatr        ISSN： 0019-5456            Impact factor:   1.967


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  1 in total

1.  Significant clinical heterogeneity with similar ETFDH genotype in three Chinese patients with late-onset multiple acyl-CoA dehydrogenase deficiency.

Authors:  Hong-Xia Fu; Xin-Yi Liu; Zhi-Qiang Wang; Ming Jin; Dan-Ni Wang; Jun-Jie He; Min-Ting Lin; Ning Wang
Journal:  Neurol Sci       Date:  2016-03-21       Impact factor: 3.307
  1 in total
  1 in total

1.  Screening of multiple acyl-CoA dehydrogenase deficiency in newborns and follow-up of patients.

Authors:  Duo Zhou; Meiling Ye; Zhenzhen Hu; Yu Zhang; Lin Zhu; Rulai Yang; Xinwen Huang
Journal:  Zhejiang Da Xue Xue Bao Yi Xue Ban       Date:  2021-08-25
  1 in total

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