Substitution at IL1RN and deletion at SLC4A11 segregating with phenotype in familial keratoconus.

Nowak, Dorota M

Substitution at IL1RN and deletion at SLC4A11 segregating with phenotype in familial keratoconus. [electronic resource] - Investigative ophthalmology & visual science Mar 2013 - 2207-15 p. digital

Publication Type: Journal Article; Research Support, Non-U.S. Gov't

1552-5783

10.1167/iovs.13-11592 doi


Amino Acid Substitution--genetics
Anion Transport Proteins--genetics
Antiporters--genetics
Asian People--genetics
DNA Mutational Analysis
Ecuador
Genetic Linkage
Humans
Interleukin 1 Receptor Antagonist Protein--genetics
Keratoconus--genetics
Mutation
Pedigree
Phenotype
Sequence Deletion