A rare neutral polymorphism in 21-hydroxylase genes as HLA haplotype marker

Author:

Narko Kirsi,Levo Antti,Partanen Jukka

Publisher

Elsevier BV

Subject

General Medicine,Immunology,Immunology and Allergy

Reference20 articles.

1. Molecular characterization of the HLA-linked steroid 21-hydroxylase B gene from an individual with congenital adrenal hyperplasia;Rodrigues;EMBO J,1987

2. Exon 7 Ncol restriction site within CYP21B (steroid 21-hydroxylase) is a normal polymorphism;Donohoue;Mol Endocrinol,1990

3. Major histocompatibility complex gene markers and restriction fragment analysis of steroid 21-hydroxylase (CYP21) and complement C4 genes in classical congenital adrenal hyperplasia patients in a single population;Partanen;Am J Hum Genet,1989

4. Ancestral haplotypes: conserved population MHC haplotypes;Degli-Esposti;Hum Immunol,1992

5. Conserved, extended MHC haplotypes;Alper;Exp Clin Immunogenet,1992

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