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Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration Volume 21, 2020 - Issue 3-4
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Letter

Rare phenotype of ALS4 associated with heterozygous missense mutation c.5842A > G/p.M1948V in helicase domain of SETX gene

I. AndreiniDepartment of Medicine, Surgery and Neurosciences, University of Siena, Siena, Italy, Correspondence[email protected]
ORCID Iconhttp://orcid.org/0000-0002-3715-0171
ORCID Icon,
F. MoroMolecular Medicine and Neurogenetics, IRCCS “Stella Maris”, Pisa, Italy,
,
L.M. AfricaDepartment of Medicine, Surgery and Neurosciences, University of Siena, Siena, Italy,
,
A. RubegniMolecular Medicine and Neurogenetics, IRCCS “Stella Maris”, Pisa, Italy,
,
F.M. SantorelliMolecular Medicine and Neurogenetics, IRCCS “Stella Maris”, Pisa, Italy,
,
C. ScarpiniUnit of Neurology, Misericordia Hospital, Grosseto, Italy
,
F. SicurelliDepartment of Medicine, Surgery and Neurosciences, University of Siena, Siena, Italy,
&
C. BattistiDepartment of Medicine, Surgery and Neurosciences, University of Siena, Siena, Italy,
show all
Pages 312-313 | Received 21 Nov 2019, Accepted 28 Feb 2020, Published online: 18 Mar 2020

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