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De novo mutations in sporadic deletional Duchenne muscular dystrophy (DMD) cases

Mukherjee , Chaturvedi LS, Srivastava S, Mittal RD, Mittal B

  • KMID: 1097259
  • Exp Mol Med.
  • 2003 Apr;35(2):113-117.
Dinucleotide repeat polymorphism based genetic analysis is a powerful approach to gain insight into rare genetic events like germline mosaicism and de novo mutations. The loss of heterozygosity of polymorphic...
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