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. 2006 May 25;174(5):590–598. doi: 10.1164/rccm.200602-165OC

Figure 3.

Figure 3.

BMPR2 cDNA (A) and genomic DNA sequence (B) of Family 67. As seen in A, cDNA sequencing identified a mutant transcript lacking exons 8 and 9. Genomic DNA sequencing (B) revealed a heterozygous G > T substitution at the first base of intron 8 (1128+1G > T), causing the aberrant splicing.