Molecular characterization and copy number of SMN1, SMN2 and NAIP in Chinese patients with spinal muscular atrophy and unrelated healthy controls

BACKGROUND: Spinal muscular atrophy (SMA) is caused by SMN1 dysfunction, and the copy number of SMN2 and NAIP can modify the phenotype of SMA. The aim of this study was to analyze the copy numbers and gene structures of SMA-related genes in Chinese SMA patients and unrelated healthy controls. METHOD...

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Detalles Bibliográficos
Autores principales: Fang, Ping, Li, Liang, Zeng, Jian, Zhou, Wan-Jun, Wu, Wei-Qing, Zhong, Ze-Yan, Yan, Ti-Zhen, Xie, Jian-Sheng, Huang, Jing, Lin, Li, Zhao, Ying, Xu, Xiang-Min
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4328246/
https://www.ncbi.nlm.nih.gov/pubmed/25888055
http://dx.doi.org/10.1186/s12891-015-0457-x

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