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Whole-genome sequencing: identification of additional pathogenic variation across the genome
This scientific commentary refers to ‘Genome sequencing identifies rare tandem repeat expansions and copy number variants in Lennox–Gastaut syndrome’, by Qaiser et al. (https://doi.org/10.1093/braincomms/fcab207).
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Oxford University Press
2021
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8634381/ https://www.ncbi.nlm.nih.gov/pubmed/34859220 http://dx.doi.org/10.1093/braincomms/fcab280 |