학술논문
Complement factor H mutations and gene polymorphisms in haemolytic uraemic syndrome: The C-257T, the A2089G and the G2881T polymorphisms are strongly associated with the disease
Document Type
Article
Author
Source
In: Human Molecular Genetics . (Human Molecular Genetics, 15 December 2003, 12(24):3385-3395)
Subject
Language
English
ISSN
09646906