Mutation Screening in the miR-183/96/182 Cluster in Patients With Inherited Retinal Dystrophy

Inherited retinal dystrophy (IRD) is a heterogenous blinding eye disease and affects more than 200,000 Americans and millions worldwide. By far, 270 protein-coding genes have been identified to cause IRD when defective. However, only one microRNA (miRNA), miR-204, has been reported to be responsible...

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Bibliografiset tiedot
Julkaisussa:Front Cell Dev Biol
Päätekijät: Xu, Shunbin, Coku, Ardian, Muraleedharan, Chithra K., Harajli, Ali, Mishulin, Eric, Dahabra, Chafic, Choi, Joanne, Garcia, William J., Webb, Kaylie, Birch, David, Goetz, Kerry, Li, Weifeng
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Frontiers Media S.A. 2020
Aiheet:
Cell and Developmental Biology
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC7785829/
https://ncbi.nlm.nih.gov/pubmed/33425925
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fcell.2020.619641
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