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Model Organisms Facilitate Rare Disease Diagnosis and Therapeutic Research
Efforts to identify the genetic underpinnings of rare undiagnosed diseases increasingly involve the use of next-generation sequencing and comparative genomic hybridization methods. These efforts are limited by a lack of knowledge regarding gene function, and an inability to predict the impact of gen...
Guardat en:
| Publicat a: | Genetics |
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| Autors principals: | , , , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Genetics Society of America
2017
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5586389/ https://ncbi.nlm.nih.gov/pubmed/28874452 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1534/genetics.117.203067 |
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