DMD基因突变概况 一个DM 或多 D基因 个外突变显子 缺失的缺重复68%失和11% 无义突变 重复10% 小的片突段变的插入和缺 失 剪接位点突变3% 7% TheimportanceofgeneticdiagnosisforDuchennemusculardystrophy.AnnemiekeAartsma-Rus,IekeBGinjaar,KateBushby2.
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Dystrophinopathy is one of the most common human monogenic diseases which results in Duchenne muscular dystrophy (DMD) and Becker muscular dystrophy (BMD). Mutations in the dystrophin gene are responsible for both DMD and BMD. However, the clinical pheno
YU, YUANXUN: 'DIG-labeled probe prepared by PCR for diagnosis of DMD gene deletion' CHINESE JOURNAL OF MEDICAL GENETICS vol. 12, no. 5, October 1995, pages 298 - 299 Attorney, Agent or Firm: PEKSUNG INTELLECTUAL PROPERTY LTD. (908 Shining Tower, 35 Xueyuan Road Haidian District, Beijing...
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New X431 DIAGUN V car inspection diagnosis equipment overseas global multi-language version $496.94 Min. order: 1 piece Easy Return Boat-shed switch water dispenser electronic weighing boat-shed rocker power button 2 feet 4 feet KCD1-101 KCD11 $0.06 - $0.09 Min. order: 2 pieces Easy Return ...