Using sno-lncRNAs as potential markers for Prader-Willi syndrome diagnosis

The genetic disorder Prader-Willi syndrome (PWS) is mainly caused by the loss of multiple paternally expressed genes in chromosome 15q11-q13 (the PWS region). Early diagnosis of PWS is essential for timely treatment, leading to effectively easing some clinical symptoms. Molecular approaches for PWS...

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Detalles Bibliográficos
Autores principales: Sun, Jiu-Ru, Yang, Liang-Zhong, Dai, Yang-Li, Wu, Huang, Li, Siqi, Xu, Yi-Feng, Huang, Youkui, Wu, Hao, Shen, Zheng, Zou, Chaochun, Chen, Ling-Ling
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2023
Materias:
Technical Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10324448/
https://www.ncbi.nlm.nih.gov/pubmed/37405372
http://dx.doi.org/10.1080/15476286.2023.2230406

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10324448/
https://www.ncbi.nlm.nih.gov/pubmed/37405372
http://dx.doi.org/10.1080/15476286.2023.2230406

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