The Utility of Long-Read Sequencing in Diagnosing Genetic Autosomal Recessive Parkinson’s Disease: a genetic screening study
Kensuke Daida, Hiroyo Yoshino, Laksh Malik, Breeana Baker et autres
Abstract Background Mutations within the genes PRKN and PINK1 are the leading cause of early onset autosomal recessive Parkinson’s disease (PD). However, the genetic cause of most early-onset PD (EOPD) cases still remains unresolved. Long-read sequencing has successfully identified many pathogenic structural …
us, jp, ca (code pays fourni par la source)
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medRxiv