Exome sequencing reveals a novel homozygous mutation in ACP33 gene in the first Italian family with SPG21

Overview of attention for article published in Journal of Neurology, July 2017

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twitter: 3 X users

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mendeley: 12 Mendeley

Summary X Dimensions citations

So far, Altmetric has seen 3 X posts from 3 X users, with an upper bound of 2,065 followers.

RT @varsome: Novel PC33 homozygous mutation https://t.co/zhCuT1ILqI in #Italian family w/t spastic #paraplegia SPG21 #neurology https://t.c…

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RT @varsome: Novel PC33 homozygous mutation https://t.co/zhCuT1ILqI in #Italian family w/t spastic #paraplegia SPG21 #neurology https://t.c…

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Novel PC33 homozygous mutation https://t.co/zhCuT1ILqI in #Italian family w/t spastic #paraplegia SPG21 #neurology https://t.co/GJY19YFewv

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