Chinese families with autosomal recessive hereditary spastic paraplegia caused by mutations in SPG11

Abstract Background Spastic paraplegia type 11 (SPG11) mutations are the most frequent cause of autosomal recessive hereditary spastic paraplegia (ARHSP). We are aiming to identify the causative mutations in SPG11 among families referred to our center with ARHSP in a Chinese population. Methods Targ...

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Бібліографічні деталі
Автори:	Xueping Chen, Jiao Liu, Qian-Qian Wei, Ru Wei Ou, Bei Cao, Xiaoqin Yuan, Yanbing Hou, Lingyu Zhang, Huifang Shang
Формат:	Artigo
Мова:	Inglês
Опубліковано:	BMC 2020-01-01
Серія:	BMC Neurology
Предмети:	Autosomal recessive hereditary spastic paraplegia Spastic paraplegia type 11 Genetic spectrum Phenotypic spectrum Autosomal-recessive juvenile amyotrophic lateral sclerosis
Онлайн доступ:	https://doi.org/10.1186/s12883-019-1593-y
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Chinese families with autosomal recessive hereditary spastic paraplegia caused by mutations in SPG11

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