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- NP895422.RApyCRFR-4HtQHz80-8-hBJ-nzmOwNchvR7g-Vikqni58130_assertion description "[Mutations in UBQLN2 and SIGMAR1 genes are rare in Korean patients with amyotrophic lateral sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP895422.RApyCRFR-4HtQHz80-8-hBJ-nzmOwNchvR7g-Vikqni58130_provenance.
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