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Emerging genetic complexity and rare genetic variants in neurodegenerative brain diseases
Knowledge of the molecular etiology of neurodegenerative brain diseases (NBD) has substantially increased over the past three decades. Early genetic studies of NBD families identified rare and highly penetrant deleterious mutations in causal genes that segregate with disease. Large genome-wide assoc...
Tallennettuna:
| Julkaisussa: | Genome Med |
|---|---|
| Päätekijät: | , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
BioMed Central
2021
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8048219/ https://ncbi.nlm.nih.gov/pubmed/33853652 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13073-021-00878-y |
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