Complement factor H deficiency and endocapillary glomerulonephritis due to paternal isodisomy and a novel factor H mutation. [electronic resource]
Producer: 20110630Description: 90-9 p. digitalISSN:- 1476-5470
- Alleles
- Blood Proteins -- genetics
- Chromosomes, Human, Pair 1 -- genetics
- Complement C3b Inactivator Proteins -- genetics
- Complement Factor H -- deficiency
- Complement Pathway, Alternative -- genetics
- Female
- Gene Expression Regulation
- Genetic Variation
- Glomerulonephritis -- genetics
- Heterozygote
- Homozygote
- Humans
- Infant
- Membrane Cofactor Protein -- genetics
- Mutation, Missense
- RNA, Messenger -- genetics
- Sequence Analysis, DNA
- Uniparental Disomy -- genetics
No physical items for this record
Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
There are no comments on this title.
Log in to your account to post a comment.