Combining rare single nucleotide and copy number variants in PRKN The number of heterozygous rare pathogenic PRKN SNVs (p.Q34fs, p.R256C and p.R275W) was not significantly different between controls ( n = 6, 0.82%) and PD cases ( n = 4, 0.5%, value of p = 0.6)
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[PDF] academia.edu Singh, Atul Pratap, et al
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