Associated Papers
Expanding the Clinical and Mutational Spectrum of Biallelic POC1A Variants: Characterization of Four Patients and a Comprehensive Review of POC1A-Related Phenotypes.
Altunoglu U et al.
Clinical Genetics, 2025
Ciliopathy due to POC1A deficiency: clinical and metabolic features, and cellular modeling.
Perge K et al.
European Journal of Endocrinology, 2024
Biallelic POC1A variants cause syndromic severe insulin resistance with muscle cramps.
Mericq V et al.
European Journal of Endocrinology, 2022
Identification of SOFT syndrome caused by a pathogenic homozygous splicing variant of POC1A: a case report.
Li G et al.
Bmc Medical Genomics, 2021
Further phenotypic features and two novel POC1A variants in a patient with SOFT syndrome: A case report.
Li S et al.
Molecular Medicine Reports, 2021
33955509 (PubMed )
Supplement: Supplementary_Data.pdf
Two novel POC1A mutations in the primordial dwarfism, SOFT syndrome: Clinical homogeneity but also unreported malformations.
Barraza-García J et al.
American Journal of Medical Genetics. Part A, 2016
Select a paper to view details