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mutations in SOD1 gene related to ALS patients
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创建时间：
2021-09-23
相关数据集
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Crystallizing soluble amyloid oligomers (AOs) presents a major challenge in studying disease-related mutations associated with amyloid diseases. The G37R mutation in superoxide dismutase 1 (SOD1) is l
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DataSheet2_Rare CYLD Variants in Chinese Patients With Amyotrophic Lateral Sclerosis.DOCX
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Haplotype sequence, frequency, and hap score in SOD1 haplotypes.
Haplotype sequence, frequency, and hap score in SOD1 haplotypes.
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Unveiling ten novel SETX mutations: implications for ALS pathogenesis and clinical diversity
To investigate the relationship between newly identified senataxin ( SETX) gene mutations and the clinical manifestation of Amyotrophic Lateral Sclerosis (ALS), enhancing understanding of the ge
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