Lataa...
Worldwide carrier frequency and genetic prevalence of autosomal recessive inherited retinal diseases
One of the major questions in human genetics is what percentage of individuals in the general population carry a disease-causing mutation. Based on publicly available information on genotypes from six main world populations, we created a database including data on 276,921 sequence variants, present...
Tallennettuna:
| Julkaisussa: | Proc Natl Acad Sci U S A |
|---|---|
| Päätekijät: | , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
National Academy of Sciences
2020
|
| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7007541/ https://ncbi.nlm.nih.gov/pubmed/31964843 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.1913179117 |
| Tagit: |
Lisää tagi
Ei tageja, Lisää ensimmäinen tagi!
|