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Analysis of a patient with early-onset Parkinson's disease and PARK7 gene variation / 中华医学遗传学杂志
Chinese Journal of Medical Genetics ; (6): 957-960, 2019.
Article in Chinese | WPRIM | ID: wpr-776768
ABSTRACT
OBJECTIVE@#To explore the genetic basis of a patient with early-onset Parkinson disease from a consanguineous family.@*METHODS@#Homozygosity mapping and Sanger sequencing of cDNA were used to identify the causative mutation.@*RESULTS@#A homozygous missense variation (c.56C>G, p.Thr19Arg) in the PARK7 gene was identified in the patient. In silico analysis suggested the c.56C>G variation to be pathogenic.@*CONCLUSION@#Homozygous c.56C>G variation of the PARK7 gene was the disease-causing variation in this family.
Subject(s)
Full text: Available Index: WPRIM (Western Pacific) Main subject: Parkinson Disease / Pedigree / Consanguinity / Mutation, Missense / Protein Deglycase DJ-1 / Genetics / Homozygote Limits: Humans Language: Chinese Journal: Chinese Journal of Medical Genetics Year: 2019 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Parkinson Disease / Pedigree / Consanguinity / Mutation, Missense / Protein Deglycase DJ-1 / Genetics / Homozygote Limits: Humans Language: Chinese Journal: Chinese Journal of Medical Genetics Year: 2019 Type: Article