Generation of three human induced pluripotent stem cell lines from retinitis pigmentosa 25 patient and two carriers but asymptomatic daughters
Retinitis Pigmentosa type 25 (RP25) is a form of inherited retinal dystrophy characterized by a progressive loss of rod photoreceptors, subsequent degeneration of cone photoreceptors, and eventually, the retinal pigment epithelium. Caused by mutations in the EYS gene, it is believed to be critical f...
Saved in:
Main Authors: | Helena Isla-Magrané, Maddalen Zufiaurre-Seijo, Miguel Ángel Zapata, Josep García-Arumí, Anna Duarri |
---|---|
Format: | Article |
Language: | English |
Published: |
Elsevier
2025-02-01
|
Series: | Stem Cell Research |
Online Access: | http://www.sciencedirect.com/science/article/pii/S187350612400343X |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Bone-spicule pattern in retinitis pigmentosa
by: Krzysztof Eder, et al.
Published: (2024-12-01) -
Angle Closure Glaucoma in Retinitis Pigmentosa
by: Chandni Pradhan, et al.
Published: (2020-01-01) -
Eye Motility Alterations in Retinitis Pigmentosa
by: Raffaele Migliorini, et al.
Published: (2015-01-01) -
Vitamins and Mineral Supplements for Retinitis Pigmentosa
by: Ying Zhao, et al.
Published: (2019-01-01) -
Macular abnormalities in retinitis pigmentosa. Management and treatment
by: Magdalena Durajczyk, et al.
Published: (2024-05-01)