SPG3A gene polymorphisms in hereditary spastic paraplegia

Objective: This study aimed to analyze the hereditary spastic paraplegia (HSP)/spastic paraplegia 3A (SPG3A) genomic structure as well as the polymorphisms in SPG3G genomic structure by comparing with the normal subjects. Methods: A total of 66 sporadic cases with HSP were collected from April 2014...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:Int J Clin Exp Pathol
Päätekijät: Li, Tian, Tu, Li, Zhang, Qian, Gu, Ran, Wang, Qian, Wang, Bingjin, Yao, Huan, Qu, Xiang, Wang, Wenqin, Tian, Jinyong
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: e-Century Publishing Corporation 2017
Aiheet:
Original Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC6965986/
https://ncbi.nlm.nih.gov/pubmed/31966859
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