Abstract
With recent advances in research on the genetics of Parkinson disease, molecular classification is increasingly possible. However, understanding the phenotypes of different parkinsonian syndromes and knowing when to test for various mutations are becoming more challenging. Originally, parkin gene mutations were identified as a cause of autosomal-recessive juvenile parkinsonism, but they also have been found in sporadic cases, particularly early-onset cases. Two research groups now report further details about the frequency of these mutations. To estimate …
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
