Case Report

Premature Moustache As Presenting Symptom of Nonclassic Congenital Adrenal Hyperplasia due to 2 Uncommon Mutations of the CYP21A2 Gene

Figure 3

Results of restriction analysis. Lane 1: molecular weight markers; lane 2: normal control; lane 3: the mother of the patient: lane 4: the patient. The wild-type sequence has a ApaI site resulting in two fragments of 152 bp and 144 bp (are not separated on the gel). The mutation destroys this site, leaving the PCR product of 296 bp uncut.
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