Whole-exome sequencing identifies novel compound heterozygous mutations in USH2A in Spanish patients with autosomal recessive retinitis pigmentosa

Whole-exome sequencing identifies novel compound heterozygous mutations in USH2A in Spanish patients with autosomal recessive retinitis pigmentosa

Bibliographic Details
Main Authors: Méndez-Vidal, Cristina, González-del Pozo, María, Vela-Boza, Alicia, Santoyo-López, Javier, López-Domingo, Francisco J., Vázquez-Marouschek, Carmen, Dopazo, Joaquin, Borrego, Salud, Antiñolo, Guillermo
Format: Online
Language:English
Published: Molecular Vision 2013
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3820429/

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3820429/

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