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

J. Foster, S. Kapoor, O. Diaz-Horta, A. Singh, C. Abad, A. Rastogi, R. Moharana, O. Tekeli, Katherina Walz, Mustafa Tekin

Research output: Contribution to journalArticle

4 Scopus citations
Original languageEnglish (US)
Pages (from-to)589-591
Number of pages3
JournalClinical Genetics
Volume86
Issue number6
DOIs
StatePublished - Dec 1 2014

ASJC Scopus subject areas

  • Genetics(clinical)
  • Genetics
  • Medicine(all)

Cite this

Foster, J., Kapoor, S., Diaz-Horta, O., Singh, A., Abad, C., Rastogi, A., Moharana, R., Tekeli, O., Walz, K., & Tekin, M. (2014). Identification of an IGSF3 mutation in a family with congenital nasolacrimal duct obstruction. Clinical Genetics, 86(6), 589-591. https://doi.org/10.1111/cge.12321