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• W2172055712 abstract "Mutations in ALS2, carrying three putative guanine exchange factor (GEF) domains, are causative for a juvenile, autosomal recessive form of amyotrophic lateral sclerosis (ALS), primary lateral sclerosis, and infantile-ascending hereditary spastic paralysis. Endogenous ALS2 is shown here to be enriched in nervous tissue and to be peripherally bound to the cytoplasmic face of endosomal membranes, an association that requires the amino-terminal RCC1 (regulator of chromatin condensation)-like GEF domain. Disease-causing mutants and a naturally truncated isoform of ALS2 are shown to be rapidly degraded when expressed in cultured human cells, including lymphocytes derived from patients with ALS2 mutations. Thus, mutations in the ALS2 gene linked to early-onset motor neuron disease uniformly produce loss of activity through decreased protein stability of this endosomal GEF." @default.
• W2172055712 created "2016-06-24" @default.
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• W2172055712 date "2003-12-10" @default.
• W2172055712 modified "2023-10-18" @default.
• W2172055712 title "Unstable mutants in the peripheral endosomal membrane component ALS2 cause early-onset motor neuron disease" @default.
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• W2172055712 doi "https://doi.org/10.1073/pnas.2635267100" @default.
• W2172055712 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/307689" @default.
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