๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Polymorphism of properdin factor B in Japanese. Description of a rare variant and data of association with HLA and C2

โœ Scribed by K. Tokunaga; C. Araki; T. Juji; K. Omoto


Publisher
Springer
Year
1982
Tongue
English
Weight
477 KB
Volume
60
Category
Article
ISSN
0340-6717

No coin nor oath required. For personal study only.


๐Ÿ“œ SIMILAR VOLUMES


Defective, deleted or converted CYP21B g
โœ N. Ghanem; J. M. Lobaccaro; C. Buresi; M. Abbal; G. Halaby; C. Sultan; G. Lefran ๐Ÿ“‚ Article ๐Ÿ“… 1990 ๐Ÿ› Springer ๐ŸŒ English โš– 922 KB

Defects in the enzyme, steroid 21-hydroxylase, result in congenital adrenal hyperplasia (CAH), a common autosomal recessive disorder of cortisol biosynthesis. The gene encoding this protein (CYP21B) and a closely linked pseudogene (CYP21A) have been mapped in the HLA complex on chromosome 6p, adjace

Association of a variant of the angioten
โœ Kobashi, Gen; Hata, Akira; Shido, Koichi; Kato, Emi-Hirayama; Yamada, Hideto; Fu ๐Ÿ“‚ Article ๐Ÿ“… 1999 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 24 KB ๐Ÿ‘ 2 views

The contribution of genetic factors to hypertension in pregnancy, including pre-eclampsia, has been well documented. The association with a common molecular variant of the angiotensinogen (AGT) gene, in which methionine (M235) is substituted for threonine (T235) at residue 235, has been reported in