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Updated: Jul 12, 2026

Navigating MARRVEL, a Web-Based Tool that Integrates Human Genomics and Model Organism Genetics Information
09:37

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Published on: August 15, 2019

SPG11: a consistent clinical phenotype in a family with homozygous spatacsin truncating mutation

Roberto Del Bo1, Alessio Di Fonzo, Serena Ghezzi

  • 1Dino Ferrari Centre, Department of Neurological Sciences, IRCCS Foundation, Ospedale Maggiore, Policlinico Mangiagalli and Regina Elena, University of Milan, Via Francesco Sforza 35, Milan 20122, Italy.

Neurogenetics
|August 25, 2007
PubMed

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