Three Novel Mutations of the Spastin Gene in Chinese Patients With Hereditary Spastic Paraplegia-Reference-Cited by-同舟云学术

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Three Novel Mutations of the Spastin Gene in Chinese Patients With Hereditary Spastic Paraplegia

Published:2004-01-01 Issue:1 Volume:61 Page:49
ISSN:0003-9942
Container-title:Archives of Neurology
language:en
Short-container-title:Arch Neurol

Author:

Tang Beisha,Zhao Guohua,Xia Kun,Pan Qian,Luo Wei,Shen Lu,Long Zhigao,Dai Heping,Zi Xiaohong,Jiang Hong

Publisher

American Medical Association (AMA)

Subject

Neurology (clinical),Arts and Humanities (miscellaneous)

Cited by 23 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Ochratoxin A as an alarming health threat for livestock and human: A review on molecular interactions, mechanism of toxicity, detection, detoxification, and dietary prophylaxis;Toxicon;2022-07

2. Genotype–phenotype associations in hereditary spastic paraplegia: a systematic review and meta-analysis on 13,570 patients;Journal of Neurology;2019-11-19

3. A de novo mosaic mutation in SPAST with two novel alternative alleles and chromosomal copy number variant in a boy with spastic paraplegia and autism spectrum disorder;European Journal of Medical Genetics;2017-10

4. Massive sequencing of 70 genes reveals a myriad of missing genes or mechanisms to be uncovered in hereditary spastic paraplegias;European Journal of Human Genetics;2017-08-23

5. Exon 8–17 deletions of SPAST in a Chinese family with hereditary spastic paraplegia: A case report and literature review;Journal of the Neurological Sciences;2015-10

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