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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Detalles Bibliográficos
Autores principales: Zhao, Hua, Yang, Lu, Dong, Yi, Wu, Zhi‐Ying
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7549591/
https://www.ncbi.nlm.nih.gov/pubmed/32729243
http://dx.doi.org/10.1002/mgg3.1438

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7549591/
https://www.ncbi.nlm.nih.gov/pubmed/32729243
http://dx.doi.org/10.1002/mgg3.1438

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