LOXL1 mutations are associated with exfoliation syndrome in patients from the midwestern United States

Letter/Communication

John H Fingert, Wallace L M Alward, Young H Kwon, Kai Wang, Luan M Streb, Val C Sheffield and Edwin M Stone

American journal of ophthalmology, Vol.144(6), pp.974-975.e1

12/2007

DOI: 10.1016/j.ajo.2007.09.034

PMID: 18036875

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Mutation

Amino Acid Oxidoreductases - genetics

Genetic Predisposition to Disease

Glaucoma, Open-Angle - genetics

Humans

Female

Genotype

Iowa - epidemiology

Male

Polymorphism, Single Nucleotide

Exfoliation Syndrome - genetics

Title: Subtitle: LOXL1 mutations are associated with exfoliation syndrome in patients from the midwestern United States
Creators: John H Fingert
Wallace L M Alward
Young H Kwon
Kai Wang
Luan M Streb
Val C Sheffield
Edwin M Stone
Resource Type: Letter/Communication
Publication Details: American journal of ophthalmology, Vol.144(6), pp.974-975.e1
DOI: 10.1016/j.ajo.2007.09.034
PMID: 18036875
NLM abbreviation: Am J Ophthalmol
ISSN: 0002-9394
eISSN: 1879-1891
Publisher: United States
Language: English
Date published: 12/2007
Academic Unit: Stead Family Department of Pediatrics; The University of Iowa Institute for Vision Research; Iowa Neuroscience Institute; Biostatistics; Medical Genetics and Genomics; Ophthalmology and Visual Sciences
Record Identifier: 9983980070002771

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