Marfan syndrome caused by a novel FBN1 mutation with associated pigmentary glaucoma.

Kuchtey J, Chang TC, Panagis L, Kuchtey RW
Am J Med Genet A. 2013 161A (4): 880-3

PMID: 23444230 · PMCID: PMC3638319 · DOI:10.1002/ajmg.a.35838

MeSH Terms (13)

Adult Base Sequence Fibrillin-1 Fibrillins Glaucoma, Open-Angle Humans Iris Male Marfan Syndrome Microfilament Proteins Mutation Pedigree Pigment Epithelium of Eye

Connections (1)

This publication is referenced by other Labnodes entities:

Links