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Absence of apparent disease causing mutations in COL5A3 in 13 patients with hypermobility Ehlers–Danlos syndrome

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  • How to cite this article: Hoffman GG, Dodson GE, Cole WG, Greenspan DS. 2008. Absence of apparent disease causing mutations in COL5A3 in 13 patients with hypermobility Ehlers–Danlos syndrome. Am J Med Genet Part A 146A:3240–3241.

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