Fig. 3From: Fatal thoracic aortic aneurysm and dissection in a large family with a novel MYLK gene mutation: delineation of the clinical phenotypeThe MYLK gene novel missense mutation, c.4471G > T, Ala1491Ser, located in exon 27. Her we show the electropherogram of a healthy control, carrier and homozygote representative patient (VI-26). This change converts a codon for alanine (GCA) to a codon for serine (TCA)Back to article page