Using data from the 100,000 Genomes Project to resolve conflicting interpretations of a recurrent TUBB2A mutation

Detalles Bibliográficos
Autores principales: Ragoussis, Vassilis, Pagnamenta, Alistair T, Haines, Rebecca L, Giacopuzzi, Edoardo, McClatchey, Martin A, Sampson, Julian R, Suri, Mohnish, Gardham, Alice, Cobben, Jan-Maarten, Osio, Deborah, Fry, Andrew E, Taylor, Jenny C
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2022
Materias:
Neurogenetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8961759/
https://www.ncbi.nlm.nih.gov/pubmed/33547136
http://dx.doi.org/10.1136/jmedgenet-2020-107528

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8961759/
https://www.ncbi.nlm.nih.gov/pubmed/33547136
http://dx.doi.org/10.1136/jmedgenet-2020-107528

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