Classical 11β-Hydroxylase Deficiency Caused by a Novel Homozygous Mutation: A Case Study and Literature Review

Mohammad N. Alsanea; Abdulmoein  Al-Agha; Mohamed Abdelmaksoud Shazly; Mohammad N. Alsanea; Abdulmoein  Al-Agha; Mohamed Abdelmaksoud Shazly

doi:10.7759/cureus.21537

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