Integrating Genetic Structural Variations and Whole-Genome Sequencing Into Clinical Neurology

Advances in genome sequencing technologies have unlocked new possibilities in identifying disease-associated and causative genetic markers, which may in turn enhance disease diagnosis and improve prognostication and management strategies. With the capability of examining genetic variations ranging f...

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Detalles Bibliográficos
Autores principales: Lin, Xin, Yang, Yuanhao, Melton, Phillip E., Singh, Vikrant, Simpson-Yap, Steve, Burdon, Kathryn P., Taylor, Bruce V., Zhou, Yuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer 2022
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10331588/
https://www.ncbi.nlm.nih.gov/pubmed/37435434
http://dx.doi.org/10.1212/NXG.0000000000200005

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10331588/
https://www.ncbi.nlm.nih.gov/pubmed/37435434
http://dx.doi.org/10.1212/NXG.0000000000200005

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