Fig. 2From: A novel delins (c.773_819+47delinsAA) mutation of the PCCA gene associated with neonatal-onset propionic acidemia: a case reportThe delins c.773_819 + 47delinsAA mutation detected in the family using Sanger sequencing. The proband and his father are heterozygous, while the mother is the same as the reference sequence. The red box shows the breakpoint locationBack to article page