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Phenotypic variance in monozygotic twins with SCA3
BACKGROUND: Spinocerebellar ataxia type 3 (SCA3) is a hereditary neurodegenerative disorder with high clinical heterogeneity. Twin study is valuable to estimate the contributions of gene and/or environment to phenotypic variance. However, SCA3 twins were extremely sparse and rarely reported. METHODS...
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| Yayımlandı: | Mol Genet Genomic Med |
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| Asıl Yazarlar: | , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
John Wiley and Sons Inc.
2020
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7549591/ https://ncbi.nlm.nih.gov/pubmed/32729243 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mgg3.1438 |
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