Congenital Adrenal Hyperplasia Caused by 21-Hydroxylase Deficiency: Its Molecular Basis and Its Remaining Therapeutic Problems

Author:

Migeon Claude J.,Donohoue Patricia A.

Publisher

Elsevier BV

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism

Reference53 articles.

1. Mutation in the CYP21B gene (Ile-172—>Asn) causes steroid 21-hydroxylase deficiency;Amor;Proc Natl Acad Sei USA,1988

2. Congenital adrenal hyperplasia: Long-term results following vaginal reconstruction;Aziz;Fertil Steril,1986

3. Congenital adrenal hyperplasia associated with the adrenogenital syndrome: An attempt to correct its disordered hormonal pattern;Bartter;J Clin Invest,1950

4. Mapping of steroid 21-hydroxylase genes adjacent to complement component C4 genes in HLA, the major histocompatibility complex in man;Carroll;Proc Natl Acad Sei USA,1985

5. Deletion of complement C4 and steroid 21-hydroxylase genes in the HLA Class III region;Carroll;EMBO J,1985

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