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Familial Parkinson disease type 5: A familial form of Parkinson disease inherited in an autosomal dominant manner due to mutation in the UCHL1 gene on chromosome 4p14. Also known as PARK5.
Familial Parkinson disease type 5: A familial form of Parkinson disease inherited in an autosomal dominant manner due to mutation in the UCHL1 gene on chromosome 4p14.
FAMILIAL PARKINSON DISEASE TYPE 5 - Complete Webpage for 'Familial Parkinson Disease Type 5'. Find Familial Parkinson Disease Type 5 on Web, Familial Parkinson Disease ...
Parkinson disease, familial, type 1 (PARK1) information including symptoms, diagnosis, misdiagnosis, treatment, causes, patient stories, videos, forums ...
Familial Parkinson disease type 1: A familial form of Parkinson disease inherited in an autosomal dominant manner due to mutation in the alpha-synuclein gene (SNCA) on ...
Symptoms of Parkinson disease, familial, Type 1 including 7 medical symptoms and signs of Parkinson disease, familial, Type 1, alternative diagnoses, misdiagnosis, and ...