Associated Papers
MYRF Variants in Patients With 46,XY Differences/Disorders of Sex Development and Literature Review.
Zhang W et al.
American Journal of Medical Genetics. Part A, 2025
CRISPR-based knockout and base editing confirm the role of MYRF in heart development and congenital heart disease.
Doering L et al.
Disease Models & Mechanisms, 2023
MYRF-related mild encephalopathy with reversible myelin vacuolization: a case report and literature review.
Yao S et al.
Frontiers in Genetics, 2023
Case Report: De novo variant in myelin regulatory factor in a Chinese child with 46,XY disorder/difference of sex development, cardiac and urogenital anomalies, and short stature.
Wang H et al.
Frontiers in Pediatrics, 2022
Crystal structure of the MyRF ICA domain with its upstream β-helical stalk reveals the molecular mechanisms underlying its trimerization and self-cleavage.
Wu P et al.
International Journal of Biological Sciences, 2021
Review of the phenotypic spectrum associated with haploinsufficiency of MYRF.
Rossetti LZ et al.
American Journal of Medical Genetics. Part A, 2019
De novo variants in congenital diaphragmatic hernia identify MYRF as a new syndrome and reveal genetic overlaps with other developmental disorders.
Qi H et al.
Plos Genetics, 2018
Refining the role of de novo protein-truncating variants in neurodevelopmental disorders by using population reference samples.
Kosmicki JA et al.
Nature Genetics, 2017
28191890 (PubMed )
Supplement: NIHMS845776-supplement-5.xlsx › Congenital_Heart_Disease
Functional mechanisms of MYRF DNA-binding domain mutations implicated in birth defects.
Fan C et al.
The Journal of Biological Chemistry, 0
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