## Abstract ## Objective To examine whether the affected firstβdegree relatives within multicase systemic sclerosis (SSc; scleroderma) families are concordant for autoantibody profile, disease type, and HLA class II haplotypes and whether clinical expression and serologic characteristics of famili
Clinical, genetic, and biochemical features of G-6PDWest Virginia
β Scribed by Corey, Seth J.; Beutler, Ernest
- Publisher
- John Wiley and Sons
- Year
- 1996
- Tongue
- English
- Weight
- 145 KB
- Volume
- 53
- Category
- Article
- ISSN
- 0361-8609
No coin nor oath required. For personal study only.
β¦ Synopsis
A new mutation of the G-6PD gene at position 910 is described. Biochemical analysis suggests that a conformational change results in the enzymatic deficiency associated with G-6PDWeS' Virg'n'a. o 1996 Wiley-Liss, Inc.
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