Does a rare mutation in PTPRA contribute to the development of Parkinson's disease in an Australian multi-incident family?

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作者： Melissa A,Hill ^[1] ; Steven R,Bentley ^[1] ; Tara L,Walker ^[2] ; George D,Mellick ^[1] ; Stephen A,Wood ^[1] ; Alex M,Sykes ^[1]

作者单位： Griffith Institute for Drug Discovery, Griffith University, Nathan, Australia. ^[1] Queensland Brain Institute, University of Queensland, St Lucia, Australia. ^[2]

主题词澳大利亚(Australia);疾病遗传易感性(Genetic Predisposition to Disease);HEK293细胞(HEK293 Cells);人类(Humans);突变(Mutation);帕金森病(Parkinson Disease);受体样蛋白质酪氨酸磷酸酶类, 4类(Receptor-Like Protein Tyrosine Phosphatases, Class 4)

DOI 10.1371/journal.pone.0271499

PMID 35900966

发布时间 2022-12-07

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PloS one

2022年17卷7期

e0271499页

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Does a rare mutation in PTPRA contribute to the development of Parkinson's disease in an Australian multi-incident family?

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Does a rare mutation in PTPRA contribute to the development of Parkinson's disease in an Australian multi-incident family?

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