We have analysed fifteen classical 21-hydroxylase deficiency families from throughout Southern Ireland and report the serologically defined HLA-A, HLA-B, HLA-Cw, HLA-DR, C4A and C4B polymorphisms that characterize the inferred disease haplotypes. Additionally, we have used a combination of short and
โฆ LIBER โฆ
MHC haplotypes and CYP21/C4 gene organisation in 21-hydroxylase deficient families from three European populations
โ Scribed by Sinnott, P.J.; Tassabehji, M.; Costigan, C.; Livieri, C.; Dyer, P.A.; Strachan, T.
- Book ID
- 122628790
- Publisher
- Elsevier Science
- Year
- 1991
- Tongue
- English
- Weight
- 85 KB
- Volume
- 32
- Category
- Article
- ISSN
- 0198-8859
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