Abstract
CYP21 and CYP11B genes have a common feature: they are "twin" genes. It seems as if doubling and subsequent drifting apart rendered these genes particularly sensitive to defect acquisition by mechanisms involving recombinatorial events. This creates specific difficulties in the molecular diagnosis of defects.
Subject
Endocrinology,General Medicine,Endocrinology, Diabetes and Metabolism
Cited by
18 articles.
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