Detection of carriers of deletions in th
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Juliana Bronzova; Albena Todorova; Luba Kalaydjieva
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Article
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1994
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Springer
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English
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Analysis of Bulgarian Duchenne/Becker muscular dystrophy (DMD/BMD) patients has demonstrated that deletions spanning exon 4 or exon 48 of the dystrophin gene account for about half of all patients, and that female relatives from these families constitute nearly 40% of all patients who require diagno