Literature DB >> 22175763

Atypical hereditary spastic paraplegia with thin corpus callosum in a Korean patient with a novel SPG11 mutation.

W T Yoon, W Y Lee, S-T Lee, J Y Ahn, C-S Ki, J W Cho.   

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Year:  2012        PMID： 22175763     DOI： 10.1111/j.1468-1331.2011.03569.x

Source DB:  PubMed          Journal:  Eur J Neurol        ISSN： 1351-5101            Impact factor:   6.089


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  2 in total

1.  Atypical late-onset hereditary spastic paraplegia with thin corpus callosum due to novel compound heterozygous mutations in the SPG11 gene.

Authors:  Maria Pia Giannoccaro; Rocco Liguori; Alessia Arnoldi; Vincenzo Donadio; Patrizia Avoni; Maria Teresa Bassi
Journal:  J Neurol       Date:  2014-07-25       Impact factor: 4.849

2.  Mild cognitive impairment in novel SPG11 mutation-related sporadic hereditary spastic paraplegia with thin corpus callosum: case series.

Authors:  Chuan Li; Qi Yan; Feng-Ju Duan; Chao Zhao; Zhuo Zhang; Ying Du; Wei Zhang
Journal:  BMC Neurol       Date:  2021-01-11       Impact factor: 2.474
  2 in total

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