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 November-December 2011  | Vol 59 | Issue 6

Original Article
Duchenne or Becker muscular dystrophy: A clinical, genetic and immunohistochemical study in China
Qian Wang, Xiaofeng Yang, Yang Yan, Nan Song, Changkun Lin, Chunlian Jin
Background and Objective: Duchenne and Becker muscular dystrophies are X-linked diseases caused by mutations in the dystrophin gene, which affect approximately 1 in 3,500 and 1 in 18,000 boys, ...
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Original Article
Identification of deletions and duplications in the Duchenne muscular dystrophy gene and female carrier status in western India using combined methods of multiplex polymerase chain reaction and multiplex ligation-dependent probe amplification
Rashna S Dastur, Munira Y Kachwala, Satish V Khadilkar, Madhuri R Hegde, Pradnya S Gaitonde
Background: The technique of multiplex ligation-dependent probe amplification (MLPA) assay is an advanced technique to identify deletions and duplications of all the 79 exons of DMD gene in pat...
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Neurology India
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