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Detection of copy number variation by SNP-allelotyping
Charcot-Marie-Tooth disease type 1A (CMT1A) is caused by an abnormal copy number variation (CNV) with a trisomy of chromosome 17p12. The increase of the DNA-segment copy number is expected to alter the allele frequency of single nucleotide polymorphism (SNP) within the duplicated region. We tested w...
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| Publicat a: | J Neurogenet |
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| Autors principals: | , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2014
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4254366/ https://ncbi.nlm.nih.gov/pubmed/24830919 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3109/01677063.2014.923884 |
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