Gelatinous drop-like corneal dystrophy in a child with developmental delay: clinicopathological features and exclusion of the M1S1 gene. [electronic resource]
Producer: 20050603Description: 198-204 p. digitalISSN:- 0950-222X
- Amyloid -- analysis
- Antigens, Neoplasm -- genetics
- Base Sequence
- Cell Adhesion Molecules -- genetics
- Cornea -- chemistry
- Corneal Dystrophies, Hereditary -- genetics
- Developmental Disabilities -- genetics
- Extracellular Matrix Proteins -- metabolism
- Female
- Humans
- Infant
- Lactoferrin -- metabolism
- Male
- Microscopy, Immunoelectron
- Pedigree
- Polymorphism, Genetic
- Sequence Analysis, DNA
- Transforming Growth Factor beta -- metabolism
No physical items for this record
Publication Type: Case Reports; Journal Article
There are no comments on this title.
Log in to your account to post a comment.