Long-Read Whole-Genome Sequencing as a Tool for Variant Detection in Inherited Retinal Dystrophies.
Saved in:
| Title: | Long-Read Whole-Genome Sequencing as a Tool for Variant Detection in Inherited Retinal Dystrophies. |
|---|---|
| Authors: | Rodilla, Cristina1,2 (AUTHOR), Núñez-Moreno, Gonzalo1,2,3 (AUTHOR), Benitez, Yolanda1,3 (AUTHOR), Rodríguez de Alba, Marta1,2,4 (AUTHOR), Blanco-Kelly, Fiona1,2,5 (AUTHOR), López-Alcojor, Aroa1 (AUTHOR), Fernández-Caballero, Lidia1,2 (AUTHOR), Perea-Romero, Irene1,2,3 (AUTHOR), Del Pozo-Valero, Marta1,2,4 (AUTHOR), García-García, Gema2,4,5 (AUTHOR), Balanzá, Mar2,4 (AUTHOR), Villaverde, Cristina1,2 (AUTHOR), Zurita, Olga1,2 (AUTHOR), Jubin, Claire5 (AUTHOR), Fund, Cedric5 (AUTHOR), Delepine, Marc5 (AUTHOR), Leduc, Aurelie5 (AUTHOR), Deleuze, Jean-François5 (AUTHOR), Millán, José M.2,4 (AUTHOR), Minguez, Pablo1,2,3 (AUTHOR) |
| Source: | International Journal of Molecular Sciences. Apr2025, Vol. 26 Issue 8, p3825. 16p. |
| Database: | Academic Search Ultimate |
|
Full text is not displayed to guests.
Login for full access.
|
|
Be the first to leave a comment!
