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• W3047762220 abstract "Mutations in SOD1 cause approximately 12-25% of familial ALS and ≈2% of apparently sporadic ALS cases. Clinical phenotypes linked to SOD1 mutations are heterogeneous and intra-familial variability of the clinical phenotype is frequently observed. SOD1 L144S mutation, identified also in Brazil, Iran and United States, is the second most frequent mutation among ALS patients in Poland. So far, 10 FALS pedigrees with SOD1 L144S mutation have been reported worldwide. The aim of the study was to establish the origin of SOD1 L144S mutation in geographically distinct populations. The clinical presentation of the Polish patients was compared with those from the previously reported populations (26 ever-reported patients). Clinically, L144S mutation is associated with both sporadic and familial ALS of relatively slow uniform course, a prevalent onset in the lower limbs, either classic or PMA presentation and a long survival time. Like in the case of other previously described SOD1 mutations, there was an intra-familial heterogeneity and reduced penetrance for ALS was observed. We propose that the L144S SOD1 mutation in the three studied populations has a common founder most likely of Polish origin." @default.
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• W3047762220 date "2020-08-10" @default.
• W3047762220 modified "2023-10-06" @default.
• W3047762220 title "Putative founder effect in the Polish, Iranian and United States populations for the L144S <i>SOD1</i> mutation associated with slowly uniform phenotype of amyotrophic lateral sclerosis" @default.
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• W3047762220 doi "https://doi.org/10.1080/21678421.2020.1803359" @default.
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