Associated Papers
Congenital glaucoma associated with high hyperopia, an ophthalmic phenotypical manifestation for GLIS3 deletion: case report and review of literature.
Almhmoudi F et al.
Ophthalmic Genetics, 2025
Case Report: Neonatal Diabetes Mellitus Caused by a Novel GLIS3 Mutation in Twins.
London S et al.
Frontiers in Endocrinology, 2021
GLIS1-3 transcription factors: critical roles in the regulation of multiple physiological processes and diseases.
Jetten AM
Cellular and Molecular Life Sciences : Cmls, 2018
Emerging roles of GLIS3 in neonatal diabetes, type 1 and type 2 diabetes.
Wen X et al.
Journal of Molecular Endocrinology, 2017
Expanding the Clinical Spectrum Associated With GLIS3 Mutations.
Dimitri P et al.
The Journal of Clinical Endocrinology and Metabolism, 2015
TRANSCRIPTION FACTOR GLI-SIMILAR 3 (GLIS3): IMPLICATIONS FOR THE DEVELOPMENT OF CONGENITAL HYPOTHYROIDISM.
Lichti-Kaiser K et al.
Journal of Endocrinology, Diabetes & Obesity, 2014
Incidence, genetics, and clinical phenotype of permanent neonatal diabetes mellitus in northwest Saudi Arabia.
Habeb AM et al.
Pediatric Diabetes, 2012
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