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Familial Parkinson disease type 6: A familial form of Parkinson disease inherited in an autosomal recessive manner due to mutation in a gene on chromosome 1p distinct from DJ1. Also known as PARK6.
Familial Parkinson disease type 6: A familial form of Parkinson disease inherited in an autosomal recessive manner due to mutation in a gene on chromosome 1p distinct from ...
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 ...
We confirmed the linkage of this type of familial Parkinson's disease to the superoxide dismutase loci that is located in the telomeric region of chromosome 6 by the ...
Symptoms of Parkinson disease, familial, Type 1 including 7 medical symptoms and signs of Parkinson disease, familial, Type 1, alternative diagnoses, misdiagnosis, and ...