Detection of dystrophin gene mutation carrier state
Bisko, M.; Zimowski, J.G.; Fidziańska, E.; Badurska, B.; Fidziańska, A.; Hausmanowa-Petrusewicz, I.; Zaremba, J.
Neurologia i Neurochirurgia Polska 30(2): 193-199; Quiz 200
1996
ISSN/ISBN: 0028-3843 PMID: 8756246 Document Number: 455347
RFLP polymorphism and the sequence of repeated CA were analysed by means of polymerase chain reaction in 62 families in which cases of DMD/BMD had occurred. The established carriers were suggested to undergo prenatal examinations for avoiding giving birth to a child with Duchenne or Becker type of muscular dystrophy.
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