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

03 medical and health sciences 0302 clinical medicine Spastic Paraplegia, Hereditary Mutation Humans Proteins
DOI: 10.4103/0028-3886.173660 Publication Date: 2016-04-27T12:20:32Z
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AUTHORS (5)
Samir Patel
PrahladKumar Sethi
Ish Anand
Anuradha Batra
Pooja Gupta
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