Clinical Study
Identification of a Mutation in the Novel Compound Heterozygous CFTR in a Chinese Family with Cystic Fibrosis
Figure 2
Pedigree of the CFTR gene in three generations of a family with cystic fibrosis (lined symbols in generation II). The male proband had a compound heterozygous mutation ( male c.400 A > G heterozygous carrier; Female c.3484 C > T heterozygous carrier; Male c.400 A > G and c.3484 C > T compound heterozygous; Female c.400 A > G and c.3484 C > T compound heterozygous).