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PDF) KIF1A missense mutations in SPG30, an autosomal recessive spastic paraplegia: distinct phenotypes according to the nature of the mutations | Gabor Gyapay - Academia.edu
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Alex Stevanin - Chief Executive Officer - SIAP+MICROS S.p.A. | LinkedIn
Alex Stevanin (alexstevanin) - Profilo | Pinterest
Stevanin – Non Ricordo di Averle Uccise: il killer e torturatore di cinque donne si confessa sul Nove | DavideMaggio.it
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Alex Stevanin - Chief Executive Officer - SIAP+MICROS S.p.A. | LinkedIn
PDF) Delving into the complexity of hereditary spastic paraplegias: how unexpected phenotypes and inheritance modes are revolutionizing their nosology
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Alex Stevanin - Chief Executive Officer - SIAP+MICROS S.p.A. | LinkedIn
Speakers - React-congress
Alex Stevanin - Chief Executive Officer - SIAP+MICROS S.p.A. | LinkedIn
Follow the news on the SPATAX/ASG meeting on spastic paraparesis and ataxias | SPATAX Network : Clinical and Genetic Analysis of Spastic paraplegia and Ataxia
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Amir Boukhris, Rebecca Schule, José L - ppt download
PDF) Mutations in SPG11, encoding spatacsin, are a major cause of spastic paraplegia with thin corpus callosum | Vítor Tedim Cruz - Academia.edu
Follow the news on the SPATAX/ASG meeting on spastic paraparesis and ataxias | SPATAX Network : Clinical and Genetic Analysis of Spastic paraplegia and Ataxia
Follow the news on the SPATAX/ASG meeting on spastic paraparesis and ataxias | SPATAX Network : Clinical and Genetic Analysis of Spastic paraplegia and Ataxia
