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Germline KRAS Mutations Cause Aberrant Biochemical and Physical Properties Leading to Developmental Disorders
The KRAS gene is the most common locus for somatic gain-of-function mutations in human cancer. Germline KRAS mutations were shown recently to be associated with developmental disorders, including Noonan syndrome (NS), cardio-facio-cutaneous syndrome (CFCS), and Costello syndrome (CS). The molecular...
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| Hoofdauteurs: | , , , , , , , |
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| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
2010
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3117284/ https://ncbi.nlm.nih.gov/pubmed/20949621 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/humu.21377 |
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