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

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作者： Ikram,Sghaier ^[1] ; Imen,Kacem ^[1] ; Nicola,Ticozzi ^[2] ; Saloua,Mrabet ^[3] ; Silvia,Paverelli ^[4] ; Youssef,Abida ^[1] ; Antonia,Ratti ^[2] ; Vincenzo,Silani ^[3] ; Riadh,Gouider ^[1]

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

主题词人类(Humans);肌萎缩侧索硬化(Amyotrophic Lateral Sclerosis);表型(Phenotype)

DOI 10.1111/cge.14205

PMID 36028943

发布时间 2022-11-21

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