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G.P.8.01 Genotype–phenotype study of cardiomyopathy in patients with LGMD2 and BMD

✍ Scribed by M. Sveen; J. Thune; L. Køber; J. Vissing


Book ID
116793016
Publisher
Elsevier Science
Year
2007
Tongue
English
Weight
46 KB
Volume
17
Category
Article
ISSN
0960-8966

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The molecular analysis of 127 DMD/BMD patients showed that 73 of them (57%) had deletions in the dystrophin gene. Two different methods were used in this study: (a) hybridization of HindIII-digested genomic DNA with nine cDNA probes corresponding to the entire 14kb cDNA of the DMD gene; and (b) simu