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Paper Details

Characterization of a distinct lethal arteriopathy syndrome in twenty-two infants associated with an identical, novel mutation in FBLN4 gene, confirms fibulin-4 as a critical determinant of human vascular elastogenesis.
Orphanet J Rare Dis
32
2012
Author NameAffiliation
Mahesh KappanayilAmrita Institute of Medical Sciences and Research Centre
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Release 1.2