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
Year: 2003
Type: article
Study design: Observational Study
Source: Human Molecular Genetics
DOI: 10.1093/hmg/ddg363
Institution: Mario Negri Institute for Pharmacological Research
Language: English
Subfield: Immunology
Field: Immunology and Microbiology
Domain: Life Sciences
Open Access status: closed
OpenAlex ID: W2128624830
