We studied 38 unrelated patients from southern France with Duchenne (DMD) or Becker (BMD) muscular dystrophy for intragenic deletions of the DMD/BMD gene. We used both multiplex amplification of selected exons and cDNA probes. Of the 26 (68%) unrelated individuals found to have deletions, 24 (92%) w
β¦ LIBER β¦
The effect of caregiving on women in families with Duchenne/Becker muscular dystrophy
β Scribed by Aileen Kenneson; Janet Kay Bobo
- Book ID
- 108776794
- Publisher
- John Wiley and Sons
- Year
- 2010
- Tongue
- English
- Weight
- 122 KB
- Volume
- 18
- Category
- Article
- ISSN
- 0966-0410
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## Introduction: Duchenne/becker muscular dystrophies (dmd/bmd) are x-linked recessive diseases caused by mutations in the dystrophin gene. ## Methods: We used multiplex polymerase chain reaction (pcr) and short tandem repeat (str) segregation analysis for dmd/bmd-carrier detection and prenatal d