Home > A. Molecular pathology > FBN2
FBN2
Wednesday 9 February 2005
Pathology
germline mutations of FBN2 in congenital contractural arachnodactyly (CCA)
See also
FBNs
microfibrils
extracellular matrix
A. Molecular pathology
- CDs
- Fusion genes
- Immunochemistry
- Metabolome
- miRNAs
- ncRNAs
- Network biology
- Signaling pathways
- tRNAs
- Variants-Mutants
Also in this section
- oncogene-induced senescence pathways
- CDKN2D
- CDKN2s
- aberrant methylation in cancer
- protein function prediction
- chromosome-centric mapping of disease-associated genes
- human interactome
- MED15
- TRPS1
- CPEB4
