机译:由于CoQ9突变引起的初级辅酶Q10缺乏案例
University of Health Sciences Dr. Sami Ulus Maternity and Children’s Research and Education;
University of Health Sciences Dr. Sami Ulus Maternity and Children’s Research and Education;
University of Health Sciences Dr. Sami Ulus Maternity and Children’s Research and Education;
University of Health Sciences Dr. Sami Ulus Maternity and Children’s Research and Education;
University of Health Sciences Dr. Sami Ulus Maternity and Children’s Research and Education;
University of Health Sciences Dr. Sami Ulus Maternity and Children’s Research and Education;
University of Health Sciences Dr. Sami Ulus Maternity and Children’s Research and Education;
Intergen Genetic Diagnosis Center Ankara Turkey;
Gazi University Hospital Department of Pediatric Metabolism and Nutrition Ankara Turkey;
cardiomyopathy; COQ9 gene; epilepsy; primary coenzyme Q10 deficiency;
机译:由于CoQ9突变引起的初级辅酶Q10缺乏案例
机译:由于CoQ8A基因突变引起的初级辅酶Q10缺乏
机译:初级辅酶Q10缺乏-7:南方南方的膨胀表型谱和创始人突变
机译:透明质酸凝胶中负载辅酶Q10的非晶态形式
机译:表征推定激酶Coq8的稳定作用和Coq9多肽在酵母辅酶Q生物合成中的功能
机译:一个无意义的COQ9突变导致常染色体隐性新生儿发作的主要辅酶Q10缺乏症:线粒体疾病的一种可能的治疗形式。
机译:一个无意义的COQ9突变导致常染色体隐性新生儿发作的主要辅酶Q10缺乏症:线粒体疾病的一种可能的治疗形式。