Mild and severe muscular dystrophy associated with deletions in Xp21 of the human X chromosome.

We have analysed over 300 patients suffering from Duchenne or Becker muscular dystrophy (DMD or BMD). Deletions have been characterised which encompass either the pERT87 (DXS164) locus only, the XJ1.1 (DXS206) and HIP25 loci only, or all three loci. These loci have been shown to lie within the DMD r...

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Detaylı Bibliyografya
Asıl Yazarlar: Davies, K E, Smith, T J, Bundey, S, Read, A P, Flint, T, Bell, M, Speer, A
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 1988
Konular:
Research Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC1015414/
https://ncbi.nlm.nih.gov/pubmed/3162536
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