Molecular detection of genetic defects in ambiguous genitalia (AG) and congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency

Molecular detection of genetic defects in ambiguous genitalia (AG) and congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency

Congenital adrenal hyperplasia (CAH) is a group of inherited disorders affecting the enzymes catalyzing the synthesis of steroids in the adrenal cortex.Malfunction of 21-hydroxylase is the most frequent defect among these disorders.This enzyme is essential for the synthesis of cortisol and aldostero...

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Bibliographic Details
Main Authors: Zain, Fuziah Md, Isa, Mohd Nizam, Awang, Rus Anida
Format: Conference or Workshop Item
Language:English
Published: 2000
Subjects:
RC648-665 Diseases of the endocrine glands. Clinical endocrinology
Online Access:http://eprints.usm.my/42517/1/GP...Molecular_Detection_Of_Genetic_Defects_In_Ambiguours_Genitalia_%28AG%29_And_Congenital_Adernal_Hyperplasia_%28CAH%29_Due_To_21-Hydroxylase_Deficiency...2000...OCR...pdf
http://eprints.usm.my/42517/
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Institution: Universiti Sains Malaysia
Language: English

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http://eprints.usm.my/42517/1/GP...Molecular_Detection_Of_Genetic_Defects_In_Ambiguours_Genitalia_%28AG%29_And_Congenital_Adernal_Hyperplasia_%28CAH%29_Due_To_21-Hydroxylase_Deficiency...2000...OCR...pdf
http://eprints.usm.my/42517/

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