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Thrombotic Microangiopathy with Complement Factor H Gene Mutations Unassociated with Atypical Hemolytic Uremic Syndrome.
- Source :
-
Turkish journal of haematology : official journal of Turkish Society of Haematology [Turk J Haematol] 2015 Sep; Vol. 32 (3), pp. 275-6. - Publication Year :
- 2015
- Subjects :
- Amino Acid Substitution
Antibodies, Monoclonal, Humanized therapeutic use
Atypical Hemolytic Uremic Syndrome drug therapy
Child, Preschool
DNA Mutational Analysis
Exons genetics
Genetic Association Studies
Genotype
Humans
Male
Protein Domains genetics
Sequence Analysis, DNA
Atypical Hemolytic Uremic Syndrome genetics
Complement Factor H genetics
Mutation, Missense
Point Mutation
Subjects
Details
- Language :
- English
- ISSN :
- 1308-5263
- Volume :
- 32
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- Turkish journal of haematology : official journal of Turkish Society of Haematology
- Publication Type :
- Editorial & Opinion
- Accession number :
- 26376595
- Full Text :
- https://doi.org/10.4274/tjh.2015.0084