Genetic study of a Chinese pedigree with early onset Parkinson’s disease caused by novel compound heterozygous mutations in PARKIN gene
Objective To explore the genetic basis for a Chinese pedigree where two siblings were affected with early‐onset Parkinson's disease (EOPD). Methods Clinical examinations and genomic analyses were performed on five subjects belonging to two generations of a Han Chinese family. Target regions cap...
| Main Authors: | , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
Wiley-VCH
2021-06-01
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| Series: | Ibrain |
| Subjects: | |
| Online Access: | https://doi.org/10.1002/j.2769-2795.2021.tb00072.x |