Deficiency of the human complement regulatory protein factor H associated with low levels of component C9. [electronic resource]
Producer: 20081007Description: 445-55 p. digitalISSN:- 1365-3083
- Base Sequence
- Blood Coagulation Disorders, Inherited -- blood
- Blotting, Western
- Child, Preschool
- Complement Activation -- physiology
- Complement C3b Inactivator Proteins
- Complement C9 -- analysis
- Complement Factor H -- deficiency
- Complement System Proteins -- analysis
- Consanguinity
- Enzyme-Linked Immunosorbent Assay
- Female
- Fibroblasts -- metabolism
- Humans
- Male
- Microscopy, Confocal
- Mutation
- Pedigree
- Pneumonia -- etiology
- Reverse Transcriptase Polymerase Chain Reaction
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Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
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