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 (Q33357336)
Jump to navigation
Jump to search
scientific article
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | 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 |
scientific article |
Statements
1 reference
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 (English)
1 reference
Jessica Caprioli
1 reference
Federica Castelletti
1 reference
Sara Bucchioni
1 reference
Paola Bettinaglio
1 reference
Elena Bresin
1 reference
Gaia Pianetti
1 reference
Sara Gamba
1 reference
Simona Brioschi
1 reference
Erica Daina
1 reference
Marina Noris
1 reference
International Registry of Recurrent and Familial HUS/TTP
1 reference
28 October 2003
1 reference
1 reference
Identifiers
1 reference