Figure 1
From: A de novo mutation of the MYH7 gene in a large Chinese family with autosomal dominant myopathy
Family pedigree of a Chinese large family with LDM. Asterisk indicates the member whose DNA sample was available. The letter S indicates a patient with severe scoliosis. Question mark indicates individual whose disease status (affected or unaffected) was unclear. The F1 member set consisting of only affected individuals is surrounded by a red line, and the F2 set consisting of affected and unaffected individuals is surrounded by a blue line.
