Fig. 2From: Splicing defect in FKBP10 gene causes autosomal recessive osteogenesis imperfecta disease: a case reporta). RT-PCR for identification of FKBP10 gene expression in several commercially available cDNAs from various human tissues. It can be seen that the expression of this gene is observed in brain, liver, kidney, heart, muscle, and lung. b). RT-PCR shows the presence of FKBP10 transcript in skin biopsy samples in the normal indivitualBack to article page