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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

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