The oligogenic model of amyotrophic lateral sclerosis; phenotypes of three Tunisian families

Clin Genet. 2022 Dec;102(6):555-556. doi: 10.1111/cge.14205. Epub 2022 Aug 26.

Ikram Sghaier¹, Imen Kacem^{1

2}, Nicola Ticozzi^{3

4}, Saloua Mrabet^{1

2}, Silvia Paverelli³, Youssef Abida^{1

2}, Antonia Ratti^{3

5}, Vincenzo Silani^{3

4}, Riadh Gouider^{1

2}

¹ Neurology Department, LR18SP03, Clinical Investigation Center (CIC) "Neurosciences and Mental Health", Razi Hospital, Tunis, Tunisia.
² Faculty of Medicine of Tunis, University Tunis El Manar, Tunis, Tunisia.
³ Department of Neurology and Laboratory of Neuroscience, Istituto Auxologico Italiano, IRCCS, Milano, Italy.
⁴ Department of Pathophysiology and Transplantation, Università degli Studi di Milano, Milano, Italy.
⁵ Department of Medical Biotechnology and Translational Medicine, Università degli Studi di Milano, Milano, Italy.

No abstract available

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