Literature DB >> 26755014

Hereditary spastic paraplegia with a thin corpus callosum due to SPG11 mutation.

Samir Patel1, Prahlad Kumar Sethi, Ish Anand, Anuradha Batra, Pooja Gupta.   

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Year:  2016        PMID： 26755014     DOI： 10.4103/0028-3886.173660

Source DB:  PubMed          Journal:  Neurol India        ISSN： 0028-3886            Impact factor:   2.117


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  2 in total

1.  Spastizin mutation in hereditary spastic paraplegia with thin corpus callosum.

Authors:  Sanjiban Chakrabarty; Nimish Vijayakumar; Kurupath Radhakrishnan; Kapaettu Satyamoorthy
Journal:  J Neurol       Date:  2016-08-20       Impact factor: 4.849

2.  Hereditary Spastic Paraplegia with Mental Impairment, Thin Corpus Callosum and Amyotrophy: A Road Map to SPG11 Contributors.

Authors:  Divya Goel; C M Sharma; B L Kumawat
Journal:  Ann Indian Acad Neurol       Date:  2020-06-10       Impact factor: 1.383
  2 in total

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