Condition: HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 1
rs121913051 in
CFH gene and
HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 1
PMID 19846853 2009 Atypical hemolytic-uremic syndrome.
PMID 19821824 2010 Clinical practice guidelines for the management of atypical haemolytic uraemic syndrome in the United Kingdom.
PMID 9551389 1998 Genetic studies into inherited and sporadic hemolytic uremic syndrome.
PMID 10762557 2000 Complement factor H gene mutation associated with autosomal recessive atypical hemolytic uremic syndrome.
PMID 10577907 1999 Complement factor H gene mutation associated with autosomal recessive atypical hemolytic uremic syndrome.
PMID 14583443 2003 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.
PMID 20513133 2010 Mutations in alternative pathway complement proteins in American patients with atypical hemolytic uremic syndrome.
PMID 11851332 2002 Molecular modelling of the C-terminal domains of factor H of human complement: a correlation between haemolytic uraemic syndrome and a predicted heparin binding site.
PMID 12960213 2003 Haemolytic uraemic syndrome and mutations of the factor H gene: a registry-based study of German speaking countries.
PMID 14978182 2004 Heterozygous and homozygous factor h deficiencies associated with hemolytic uremic syndrome or membranoproliferative glomerulonephritis: report and genetic analysis of 16 cases.