Nonetheless, several new mutations (DNAJC13 (R1382H) (Lin et al. 2019), DNAJC13(D1670G) (Li et al. 2020); DNAJC13(S1608R) (Gialluisi et al. 2021), DNAJC13(R903K) (Gagliardi et al. 2018), DNAJC13(R1830C) (Trinh et al. 2019) had been identified to cause PD in cohorts of different ethnicities in an autosomal‐dominant inheritance fashion. The gene discussed is DNAJC13; the disease is Parkinson disease.