Identification of an IGSF3 mutation in a family with congenital nasolacrimal duct obstruction

Clin Genet. 2014 Dec;86(6):589-91. doi: 10.1111/cge.12321. Epub 2013 Dec 27.

Authors

J Foster 2nd¹, S Kapoor, O Diaz-Horta, A Singh, C Abad, A Rastogi, R Moharana, O Tekeli, K Walz, M Tekin

Affiliation

¹ Dr. John T. Macdonald Foundation Department of Human Genetics and John P. Hussman Institute for Human Genomics, University of Miami Miller School of Medicine, Miami, FL, USA.

PMID: 24372406
DOI: 10.1111/cge.12321

No abstract available

Publication types

Case Reports
Letter
Research Support, Non-U.S. Gov't

MeSH terms

Child
Child, Preschool
Female
Humans
Immunoglobulins / genetics*
Lacrimal Duct Obstruction / genetics*
Male
Membrane Proteins / genetics*
Mutation*
Nasolacrimal Duct / abnormalities*
Pedigree

Substances

IGSF3 protein, human
Immunoglobulins
Membrane Proteins