New spastic paraplegia phenotype associated to mutation of NFU1

Overview of attention for article published in Orphanet Journal of Rare Diseases, February 2015

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A mutation has been linked to new spastic paraplegia phenotype http://t.co/2fuvZmCdar - new in OJRD #raredisease

#ngs #sequencing New spastic paraplegia phenotype associated to mutation of NFU1 http://t.co/yroBSwZwzJ

New spastic paraplegia phenotype associated to mutation of NFU1 http://t.co/LD3bwMcNPb

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