A Case of Intracranial Hemorrhage in a Neonate with Osteogenesis Imperfecta Type III with a Novel Mutation in COL1A2 : Figure 2

Figure 2: Mutation analysis of the COL1A2 gene. Electropherograms of the affected patient, the father and a control are shown. The arrow marks the heterozygous c.1036-2A>C, splicing variant at IVS19 of COL1A2.