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Missense mutations of conserved glycine residues in fibrillin-1 highlight a potential subtype of cb-EGF-like domains
Human Mutation, 10/12/09
Van Kien PK et al. – The data compared with those of the literature strongly suggest the existence of a cb–EGF domain subtype with implications for related diseases.
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Purinergic mechanosensory transduction and visceral pain
Molecular Pain, 11/30/09
APOE and ACE polymorphisms and dementia risk in the older population over prolonged follow-up: 10 years of incidence in the MRC CFA Study
Age and Aging, 11/30/09
OCRL1 function in renal epithelial membrane traffic
American Journal of Physiology: Renal Physiology, 11/30/09
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