Visualitza per autor "HERNAN SENDRA, IMMA"
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Mutant PRPF8 Causes Widespread Splicing Changes in Spliceosome Components in Retinitis Pigmentosa Patient iPSC-Derived RPE Cells
Arzalluz-Luque, Angeles; Cabrera, Jose-Luis; Skottman, Heli; Benguria, Alberto; Bolinches-Amorós, Arantxa; Cuenca, Nicolas; Delas, Barbara; Carballo, Miguel; Pascual, Beatriz ; HERNAN SENDRA, IMMA (Frontiers Media, 2021-04-29) -
Next-generation sequencing-based gene panel tests for the detection of rare variants and hypomorphic alleles associated with primary open-angle glaucoma
MILLA, ELENA; Laguna, Javier; Alforja, Socorro; Pascual, Beatriz; GAMUNDI RODRIGUEZ, MARIA JOSE; Borràs, Emma; Carballo, Miguel; HERNAN SENDRA, IMMA (Public Library of Science, 2024-01-19) -
Next-generation sequencing-based gene panel tests for the detection of rare variants and hypomorphic alleles associated with primary open-angle glaucoma
Laguna, Javier; Pascual, Beatriz; GAMUNDI RODRIGUEZ, MARIA JOSE; Borras, Emma; Carballo, Miguel; MILLA, ELENA; Alforja, Socorro; HERNAN SENDRA, IMMA (Public Library of Science, 2024-01-19)