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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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Autors principals: Tsumagari, K, Chen, D, Hackman, J R, Bossler, A D, Ehrlich, M
Format: Artigo
Idioma:Inglês
Publicat: 2010
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Accés en línia: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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