Analysis of dystrophin gene deletions by multiplex PCR in eastern India

The most common genetic neuromuscular disease of childhood, Duchenne and Becker muscular dystrophy (DMD/BMD) is caused by deletion, duplication or point mutation of the dystrophin gene located at Xp 21.2. In the present study DNA from seventy unrelated patients clinically diagnosed as having DMD/BMD...

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Veröffentlicht in:	Neurology India 2006-07, Vol.54 (3), p.310-311
Hauptverfasser:	Basak, Jayasri, Dasgupta, Uma B, Banerjee, Tapas K, Senapati, Asit K, Das, Shyamal K, Mukherjee, Subhash C
Format:	Artikel
Sprache:	eng
Schlagworte:	Age of Onset Diagnosis Dystrophin - genetics Exons Female Gene Deletion Gene mutations Genetic research Humans India - epidemiology Male Muscular Dystrophy, Duchenne - epidemiology Muscular Dystrophy, Duchenne - genetics Polymerase chain reaction Polymerase Chain Reaction - methods RNA, Messenger - metabolism
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