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Editorial : molecular mechanisms of heritable connective tissue disorders
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Defective proteolytic processing of fibrillar procollagens and prodecorin due to biallelic BMP1 mutations results in a severe, progressive form of osteogenesis imperfecta
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Thoracic aortic-aneurysm and dissection in association with significant mitral valve disease caused by mutations in TGFB2
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Identification of binding partners interacting with the α1-N-propeptide of type V collagen