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dc.contributor.authorFarrugia Wismayer, Maia-
dc.contributor.authorFarrugia Wismayer, Andrew-
dc.contributor.authorPace, Adrian-
dc.contributor.authorVassallo, Neville-
dc.contributor.authorCauchi, Ruben J.-
dc.date.accessioned2022-02-03T16:10:20Z-
dc.date.available2022-02-03T16:10:20Z-
dc.date.issued2021-
dc.identifier.citationFarrugia Wismayer, M., Farrugia Wismayer, A., Pace, A., Vassallo, N., & Cauchi, R. J. (2021). SOD1 D91A variant in the southernmost tip of Europe: a heterozygous ALS patient resident on the island of Gozo. European Journal of Human Genetics, 1–4en_GB
dc.identifier.urihttps://www.um.edu.mt/library/oar/handle/123456789/88271-
dc.description.abstractAmyotrophic lateral sclerosis (ALS) is frequently caused by mutations in the SOD1 gene. Here, we report the first SOD1 variant in Malta, an archipelago of three inhabited islands in southern Europe. We describe a patient with a sporadic form of ALS living on the island of Gozo in which the heterozygous SOD1 c.272A>C; p.(Asp91Ala) variant was detected. The patient had a late onset (79 years), sensory impairments and rapid disease progression culminating in respiratory failure. ALS has not yet developed in any of the three additional family members in which the D91A variant was identified. None of the healthy controls from the Maltese population were found to carry this variant. This report underscores the high prevalence of the D91A variant in Europe, despite the presence of a North-South gradient in its frequency, and confirms that this variant can be associated with dominant cases in Mediterranean countries.en_GB
dc.language.isoenen_GB
dc.publisherNature Publishing Groupen_GB
dc.rightsinfo:eu-repo/semantics/openAccessen_GB
dc.subjectAmyotrophic lateral sclerosisen_GB
dc.subjectSuperoxide dismutaseen_GB
dc.subjectMotor neuronsen_GB
dc.titleSOD1 D91A variant in the southernmost tip of Europeb: a heterozygous ALS patient resident on the island of Gozoen_GB
dc.typearticleen_GB
dc.rights.holderThe copyright of this work belongs to the author(s)/publisher. The rights of this work are as defined by the appropriate Copyright Legislation or as modified by any successive legislation. Users may access this work and can make use of the information contained in accordance with the Copyright Legislation provided that the author must be properly acknowledged. Further distribution or reproduction in any format is prohibited without the prior permission of the copyright holderen_GB
dc.description.reviewedpeer-revieweden_GB
dc.identifier.doi10.1038/s41431-021-00975-x-
dc.publication.titleEuropean Journal of Human Geneticsen_GB
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