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1 Hereditary spastic paraplegia with thin corpus callosum due to novel homozygous mutation in SPG11 gene
Sa-Yoon Kang, Joong Goo Kim, Jung Hwhan Oh
Ann Clin Neurophysiol.2020;22(2):121-124.   Published online 2020 October 28     DOI: http://dx.doi.org/10.14253/acn.2020.22.2.121
      
2 Identification of a Heterozygous SPG11 Mutation by Clinical Exome Sequencing in a Patient With Hereditary Spastic Paraplegia: A Case Report
Ja-Young Oh, Hyun Jung Do, Seungok Lee, Ja-Hyun Jang, Eun-Hae Cho, Dae-Hyun Jang
Ann Rehabil Med.2016;40(6):1129-1134.   Published online 2016 December 30     DOI: http://dx.doi.org/10.5535/arm.2016.40.6.1129
      
3 Mutation analysis of SPAST, ATL1, and REEP1 in Korean Patients with Hereditary Spastic Paraplegia
Tae-Hyoung Kim, Jae-Hyeok Lee, Young-Eun Park, Jin-Hong Shin, Tai-Seung Nam, Hyang-Sook Kim, Ho-Jung Jang, Artem Semenov, Sang Jin Kim, Dae-Seong Kim
J Clin Neurol.2014;10(3):257-261.   Published online 2014 July 3     DOI: http://dx.doi.org/10.3988/jcn.2014.10.3.257
      
4 Thinning of the Corpus Callosum and Cerebellar Atrophy is Correlated with Phenotypic Severity in a Family with Spastic Paraplegia Type 11
Sanjeev Rajakulendran, Coro Paisán-Ruiz, Henry Houlden
J Clin Neurol.2011;7(2):102-104.   Published online 2011 June 28     DOI: http://dx.doi.org/10.3988/jcn.2011.7.2.102
      

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