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Rieger syndrome is associated with PAX6 deletion

200172 citationsJournal Articlebronze Open Access

Authors

Ruth Riise · Inland Hospital

Kari Storhaug · University of Oslo

Karen Brøndum‐Nielsen · Kennedy Center

Abstract

Rieger syndrome can -- in addition to PITX2 gene mutations and abnormalities at chromosome 13q14 -- be associated with PAX6 gene abnormalities.

Topics & Keywords

dental development and anomalies Cleft Lip and Palate Research Oral and Maxillofacial Pathology

UN Sustainable Development Goals

Life below water

Publication Details

Published in: Acta Ophthalmologica Scandinavica

Volume 79, Issue 2, pp. 201-203

DOI: 10.1034/j.1600-0420.2001.079002201.x

Field-Weighted Citation Impact: 1.35

Rieger syndrome is associated with PAX6 deletion | Researchclopedia