Applying Protein–Protein Interactions and Complex Networks to Identify Novel Genes in Retinitis Pigmentosa Pathogenesis

Retinitis Pigmentosa (RP) is a hereditary retinal disorder that causes the atrophy of photoreceptor rod cells. Since individual defective genes converge on the same disease, we hypothesized that all causal genes of RP belong in a complex network. To explore this hypothesis, we conducted a gene conne...

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Detalles Bibliográficos
Autores principales: Yoon, Su-Bin, Ma, Yu-Chien (Calvin), Venkat, Akaash, Liu, Chun-Yu (Audi), Zheng, Jie J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8999418/
https://www.ncbi.nlm.nih.gov/pubmed/35409321
http://dx.doi.org/10.3390/ijms23073962

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8999418/
https://www.ncbi.nlm.nih.gov/pubmed/35409321
http://dx.doi.org/10.3390/ijms23073962

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