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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Bibliografski detalji
Glavni autori: Davies, K E, Smith, T J, Bundey, S, Read, A P, Flint, T, Bell, M, Speer, A
Format: Artigo
Jezik:Inglês
Izdano: 1988
Teme:
Research Article
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC1015414/
https://ncbi.nlm.nih.gov/pubmed/3162536
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