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

doi:10.1111/cge.12321

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

Hussman Institute for Human Genomics

Research output: Contribution to journal › Article

4 Scopus citations

Original language	English (US)
Pages (from-to)	589-591
Number of pages	3
Journal	Clinical Genetics
Volume	86
Issue number	6
DOIs	https://doi.org/10.1111/cge.12321
State	Published - Dec 1 2014

ASJC Scopus subject areas

Genetics(clinical)
Genetics
Medicine(all)

Access to Document

10.1111/cge.12321

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

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