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Page 1
Heterozygous DHTKD1 Variants in Two European Cohorts of Amyotrophic Lateral Sclerosis Patients.
Genes (Basel). 2021 Dec 29;13(1):84. doi: 10.3390/genes13010084.
Genes (Basel). 2021.
PMID: 35052424
Free PMC article.
SPG7 mutations in amyotrophic lateral sclerosis: a genetic link to hereditary spastic paraplegia.
Osmanovic A, Widjaja M, Förster A, Weder J, Wattjes MP, Lange I, Sarikidi A, Auber B, Raab P, Christians A, Preller M, Petri S, Weber RG.
Osmanovic A, et al. Among authors: widjaja m.
J Neurol. 2020 Sep;267(9):2732-2743. doi: 10.1007/s00415-020-09861-w. Epub 2020 May 23.
J Neurol. 2020.
PMID: 32447552
Free PMC article.
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A SUMO4 initiator codon variant in amyotrophic lateral sclerosis reduces SUMO4 expression and alters stress granule dynamics.
Osmanovic A, Förster A, Widjaja M, Auber B, Das AM, Christians A, Brand F, Petri S, Weber RG.
Osmanovic A, et al. Among authors: widjaja m.
J Neurol. 2022 Sep;269(9):4863-4871. doi: 10.1007/s00415-022-11126-7. Epub 2022 May 3.
J Neurol. 2022.
PMID: 35503374
Free PMC article.
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