Spinal muscular atrophy diagnosis and carrier screening from genome sequencing data

PURPOSE: Spinal muscular atrophy (SMA), caused by loss of the SMN1 gene, is a leading cause of early childhood death. Due to the near identical sequences of SMN1 and SMN2, analysis of this region is challenging. Population-wide SMA screening to quantify the SMN1 copy number (CN) is recommended by th...

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Detalles Bibliográficos
Autores principales: Chen, Xiao, Sanchis-Juan, Alba, French, Courtney E., Connell, Andrew J., Delon, Isabelle, Kingsbury, Zoya, Chawla, Aditi, Halpern, Aaron L., Taft, Ryan J., Bentley, David R., Butchbach, Matthew E. R., Raymond, F. Lucy, Eberle, Michael A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group US 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7200598/
https://www.ncbi.nlm.nih.gov/pubmed/32066871
http://dx.doi.org/10.1038/s41436-020-0754-0

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7200598/
https://www.ncbi.nlm.nih.gov/pubmed/32066871
http://dx.doi.org/10.1038/s41436-020-0754-0

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