Mutational analysis of compound heterozygous mutation p.Q6X/p.H232R in SRD5A2 causing 46,XY disorder of sex development

Overview of attention for article published in Italian Journal of Pediatrics, March 2022

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H232R ysis of compound heterozygous mutation p.Q6X/p.H232R in SRD5A2 causing 46,XY disorder of sex development https://t.co/q49Tf3Y8qw https://t.co/t9KLLr3nuC

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