Clinical features and genotype-phenotype correlation analysis in patients with ATL1 mutations: A literature reanalysis

BACKGROUND: The hereditary spastic paraplegias (HSPs) are a group of clinically and genetically heterogeneous disorders. Approximately 10% of the autosomal dominant (AD) HSPs (ADHSPs) have the spastic paraplegia 3A (SPG3A) genotype which is caused by ATL1 gene mutations. Currently there are more tha...

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Detalles Bibliográficos
Autores principales: Zhao, Guo-hua, Liu, Xiao-min
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5379717/
https://www.ncbi.nlm.nih.gov/pubmed/28396731
http://dx.doi.org/10.1186/s40035-017-0079-3

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5379717/
https://www.ncbi.nlm.nih.gov/pubmed/28396731
http://dx.doi.org/10.1186/s40035-017-0079-3

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