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FSH dystrophy and a subtelomeric 4q haplotype: a new assay and associations with disease
BACKGROUND: Facioscapulohumeral muscular dystrophy (FSHD) is an autosomal dominant disease associated with contraction of arrays of tandem 3.3-kb units (D4Z4) on subtelomeric 4q. Disease-linked arrays usually have fewer than 11 repeat units. Equally short D4Z4 arrays at subtelomeric 10q are not link...
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| Hauptverfasser: | , , , , |
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| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
2010
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3043595/ https://ncbi.nlm.nih.gov/pubmed/20710047 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmg.2009.076703 |
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