Willoughby, Colin Eric, University of Liverpool, Department of Eye and Vision Science, Institute of Ageing and Chronic Disease, Liverpool, UK., United States
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Investigación Clínica Vol. 58 No. 1 - Reporte de Caso
A c.3037G>A mutation in FBN1 gene causing Marfan syndrome with an atypically severe phenotype.
Abstract PDF (Español (España))