Associated Papers
FAM20C and FAM20A in normal and ectopic mineralization: A focus on oro-renal syndromes.
Baker A et al.
Matrix Biology : Journal of the International Society for Matrix Biology, 2025
Potential Role of Protein Kinase FAM20C on the Brain in Raine Syndrome, an In Silico Analysis.
Palma-Lara I et al.
International Journal of Molecular Sciences, 2023
Compound heterozygous FAM20C gene variants in a patient with severe Raine syndrome: a case report.
Chirteș C et al.
Frontiers in Genetics, 2023
Raine syndrome: Report of a novel mutation and review of the different antenatal imaging modalities used to diagnose this disease.
Rameh G et al.
Prenatal Diagnosis, 2022
FAM20C Overview: Classic and Novel Targets, Pathogenic Variants and Raine Syndrome Phenotypes.
Palma-Lara I et al.
International Journal of Molecular Sciences, 2021
Recurrent variant c.1680C>A in FAM20C gene and genotype-phenotype correlation in a patient with Raine syndrome: a case report.
Bajaj S et al.
Bmc Pediatrics, 2021
Raine Syndrome, a Rare Lethal Osteosclerotic Bone Dysplasia: Prenatal Diagnosis With 3-Dimensional Ultrasound and a Postnatal Clinical Exome Evaluation.
Lulla C et al.
Journal of Ultrasound in Medicine : Official Journal of the American Institute of Ultrasound in Medicine, 2021
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