Fig. 2From: A novel nonsense mutation in ARMC5 causes primary bilateral macronodular adrenocortical hyperplasiaGenetic diagnosis of PBMAH in the proband and his offspring. a Family tree of the patient. The arrow indicates the proband. b Sanger sequencing of ARMC5 in peripheral blood samples of the patient and his offspring. c The second mutation (c.1369C>T) was identified from one out of two resected nodulesBack to article page