Pushing the genetic frontier with facioscapulohumeral muscular dystrophy
- PMID: 17310022
- DOI: 10.1212/01.wnl.0000255905.72867.ec
Pushing the genetic frontier with facioscapulohumeral muscular dystrophy
Comment on
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Expression profile of FSHD supports a link between retinal vasculopathy and muscular dystrophy.Neurology. 2007 Feb 20;68(8):569-77. doi: 10.1212/01.wnl.0000251269.31442.d9. Epub 2006 Dec 6. Neurology. 2007. PMID: 17151338
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Genotype-phenotype study in an FSHD family with a proximal deletion encompassing p13E-11 and D4Z4.Neurology. 2007 Feb 20;68(8):578-82. doi: 10.1212/01.wnl.0000254991.21818.f3. Epub 2007 Jan 17. Neurology. 2007. PMID: 17229919
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