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Identification of a novel SOD1 variant in a Chinese patient with amyotrophic lateral sclerosis / 中华医学遗传学杂志
Article 在 Zh | WPRIM | ID: wpr-922029
Responsible library: WPRO
ABSTRACT
OBJECTIVE@#To explore the genetic basis for a Chinese patient with amyotrophic lateral sclerosis (ALS).@*METHODS@#Peripheral blood samples were collected from the patient and his parents for the extraction of genomic DNA. Genetic variant was identified by whole exome sequencing. Candidate variant was verified by Sanger sequencing of his parents and healthy controls.@*RESULTS@#The patient was found to harbor a heterozygous c.420C>G (p.Asn140Lys) variant of the SOD1 gene. The same variant was not detected in his parents and 100 healthy controls. The variant has not been included in HGMD, dbSNP and other databases.@*CONCLUSION@#The c.420C>G variant of the SOD1 gene may underlie the ALS in this patient. Above finding has enriched the spectrum of SOD1 gene variants.
Subject(s)
全文: 1 索引: WPRIM 主要主题: China / Superoxide Dismutase-1 / Exome Sequencing / Heterozygote / Amyotrophic Lateral Sclerosis 研究类型: Diagnostic_studies / Prognostic_studies 限制: Humans 国家/地区名称主题: Asia 语言: Zh 期刊: Chinese Journal of Medical Genetics 年: 2021 类型: Article
全文: 1 索引: WPRIM 主要主题: China / Superoxide Dismutase-1 / Exome Sequencing / Heterozygote / Amyotrophic Lateral Sclerosis 研究类型: Diagnostic_studies / Prognostic_studies 限制: Humans 国家/地区名称主题: Asia 语言: Zh 期刊: Chinese Journal of Medical Genetics 年: 2021 类型: Article