Analysis of a family with mitochondrial trifunctional protein deficiency caused by HADHA gene mutations

Author:

Yang Jinling1,Yuan Dejian1,Tan Xiaohui2,Zeng Yexi3,Tang Ning1,Chen Dayu1,Tan Jianqiang1,Cai Ren1,Huang Jun1,Yan Tizhen1

Affiliation:

1. Newborn Screening Center, Department of Medical Genetics, Key Laboratory of Prevention and Control of Birth Defects, Liuzhou Maternity and Child Health Care Hospital, Affiliated Maternity Hospital and Affiliated Children's Hospital of Guangxi University of Science and Technology, Liuzhou, Guangxi 545000, P.R. China

2. School of Forensic Medicine, Southern Medical University, Guangzhou, Guangdong 510515, P.R. China

3. Newborn Screening Center, Huizhou Second Maternity and Child Health Care Hospital, Huizhou, Guangdong 516001, P.R. China

Publisher

Spandidos Publications

Subject

Cancer Research,Oncology,Genetics,Molecular Biology,Molecular Medicine,Biochemistry

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