Associated Papers
A novel small deletion in CWC27 gene associated with CWC27-related spliceosomeopathy.
Li H et al.
Ophthalmic Genetics, 2024
Whole-exome mutational landscape of neuroendocrine carcinomas of the gallbladder.
Liu F et al.
Signal Transduction and Targeted Therapy, 2021
33563892 (PubMed )
Supplement: 41392_2020_412_MOESM17_ESM.xlsx › Supplementary_Table_S16
Expanding the clinical and molecular spectrum of the CWC27-related spliceosomopathy.
Brea-Fernández AJ et al.
Journal of Human Genetics, 2019
Mutations in the Spliceosome Component CWC27 Cause Retinal Degeneration with or without Additional Developmental Anomalies.
Xu M et al.
American Journal of Human Genetics, 2017
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