Associated Papers
The phenotypic spectrum associated with OTX2 mutations in humans.
Gregory LC et al.
European Journal of Endocrinology, 2021
Genetic diagnosis of congenital hypopituitarism by a target gene panel: novel pathogenic variants in GLI2, OTX2 and GHRHR.
Nakaguma M et al.
Endocrine Connections, 2019
The homeobox gene Otx2 in development and disease.
Beby F et al.
Experimental Eye Research, 2013
A novel OTX2 mutation in a patient with combined pituitary hormone deficiency, pituitary malformation, and an underdeveloped left optic nerve.
Gorbenko Del Blanco D et al.
European Journal of Endocrinology, 2012
OTX2 microphthalmia syndrome: four novel mutations and delineation of a phenotype.
Schilter KF et al.
Clinical Genetics, 2011
A novel loss-of-function mutation in OTX2 in a patient with anophthalmia and isolated growth hormone deficiency.
Ashkenazi-Hoffnung L et al.
Human Genetics, 2010
Heterozygous mutations of OTX2 cause severe ocular malformations.
Ragge NK et al.
American Journal of Human Genetics, 2005
Hypomorphic variants in inherited retinal and ocular diseases: A review of the literature with clinical cases.
Thuma TBT et al.
Survey of Ophthalmology, 0
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