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Please use this identifier to cite or link to this item: https://doi.org/10.1002/mds.21206
DC FieldValue
dc.titleLRRK2 G2019S founder haplotype in the Chinese population
dc.contributor.authorTan E.-K.
dc.contributor.authorSkipper L.
dc.contributor.authorTan L.
dc.contributor.authorLiu J.-J.
dc.date.accessioned2018-12-13T01:27:30Z
dc.date.available2018-12-13T01:27:30Z
dc.date.issued2007
dc.identifier.citationTan E.-K., Skipper L., Tan L., Liu J.-J. (2007). LRRK2 G2019S founder haplotype in the Chinese population. Movement Disorders 22 (1) : 105-107. ScholarBank@NUS Repository. https://doi.org/10.1002/mds.21206
dc.identifier.issn08853185
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/149825
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentDUKE-NUS MEDICAL SCHOOL
dc.description.doi10.1002/mds.21206
dc.description.sourcetitleMovement Disorders
dc.description.volume22
dc.description.issue1
dc.description.page105-107
dc.published.statepublished
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