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Using Structural Analysis In Silico to Assess the Impact of Missense Variants in MEN1
Despite the rapid expansion in recent years of databases reporting either benign or pathogenic genetic variations, the interpretation of novel missense variants remains challenging, particularly for clinical or genetic testing laboratories where functional analysis is often unfeasible. Previous stud...
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| Publicado en: | J Endocr Soc |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Endocrine Society
2019
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6846327/ https://ncbi.nlm.nih.gov/pubmed/31737856 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/js.2019-00260 |
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