Aortic carboxypeptidase-like protein mutations and Ehlers-Danlos syndrome
Ehlers-Danlos Syndrome (EDS) comprises a spectrum of heritable connective tissue disorders with varying genetic origins and clinical manifestations such as soft tissue fragility and skin hyperextensibility. There are multiple EDS subtypes, the first few of which were defined by collagen mutations. M...
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| Language: | en_US |
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2019
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| Online Access: | https://hdl.handle.net/2144/36690 |