Associated Papers
Case Report: Identification of a novel PRR12 variant in a Chinese boy with developmental delay and short stature.
Liu Z et al.
Frontiers in Pediatrics, 2024
38798311 (PubMed )
Supplement: Table1.xlsx › Sheet1
Genotype-Phenotype Correlations in Relation to Newly Emerging Monogenic Forms of Autism Spectrum Disorder and Associated Neurodevelopmental Disorders: The Importance of Phenotype Reevaluation after Pangenomic Results.
Lintas C et al.
Journal of Clinical Medicine, 2021
Haploinsufficiency of PRR12 causes a spectrum of neurodevelopmental, eye, and multisystem abnormalities.
Chowdhury F et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2021
Dominant variants in PRR12 result in unilateral or bilateral complex microphthalmia.
Reis LM et al.
Clinical Genetics, 2021
De novo apparent loss-of-function mutations in PRR12 in three patients with intellectual disability and iris abnormalities.
Leduc MS et al.
Human Genetics, 2018
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