[Correspondence] and Parkinson’s disease—Authors’ reply
We thank Jansen and colleagues for their interest in our Article and for replicating the analysis of CHCHD2 variants using a large western European cohort from the International Parkinson's Disease Genomics Consortium (IPDGC). We reported three potentially pathogenic mutations (182C>T, Thr61Ile; 434G>A, Arg145Gln; and 300+5G>A) for autosomal dominant Parkinson's disease.1 Of these mutations, only Thr61Ile was confirmed to cosegregate in two independent families with autosomal dominant Parkinson's disease.
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