Article Versions Notes

Damián A, Ionescu RO, Rodríguez de Alba M, Tamayo A, Trujillo-Tiebas MJ, Cotarelo-Pérez MC, Pérez Rodríguez O, Villaverde C, de la Fuente L, Romero R, et al. Fine Breakpoint Mapping by Genome Sequencing Reveals the First Large X Inversion Disrupting the NHS Gene in a Patient with Syndromic Cataracts. International Journal of Molecular Sciences. 2021; 22(23):12713. https://doi.org/10.3390/ijms222312713

Damián, Alejandra, Raluca Oancea Ionescu, Marta Rodríguez de Alba, Alejandra Tamayo, María José Trujillo-Tiebas, María Carmen Cotarelo-Pérez, Olga Pérez Rodríguez, Cristina Villaverde, Lorena de la Fuente, Raquel Romero, and et al. 2021. "Fine Breakpoint Mapping by Genome Sequencing Reveals the First Large X Inversion Disrupting the NHS Gene in a Patient with Syndromic Cataracts" International Journal of Molecular Sciences 22, no. 23: 12713. https://doi.org/10.3390/ijms222312713

Damián, A., Ionescu, R. O., Rodríguez de Alba, M., Tamayo, A., Trujillo-Tiebas, M. J., Cotarelo-Pérez, M. C., Pérez Rodríguez, O., Villaverde, C., de la Fuente, L., Romero, R., Núñez-Moreno, G., Mínguez, P., Ayuso, C., & Cortón, M. (2021). Fine Breakpoint Mapping by Genome Sequencing Reveals the First Large X Inversion Disrupting the NHS Gene in a Patient with Syndromic Cataracts. International Journal of Molecular Sciences, 22(23), 12713. https://doi.org/10.3390/ijms222312713