Drugs Information Online
Drugs and diseases reference index
 |
EN |
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 chromosome 4q21. Also known as PARK1.
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 ...
Parkinson disease, familial, type 1 (PARK1) information including symptoms, diagnosis, misdiagnosis, treatment, causes, patient stories, videos, forums ...
Symptoms of Parkinson disease, familial, type 1 (PARK1) including 54 medical symptoms and signs of Parkinson disease, familial, type 1 (PARK1), alternative ...
3-Methylglutaconic Aciduria Type 3; 46 ... Parkinson disease affects more than 1% of 55-year-old individuals and ... are not a common cause of familial or Parkinson disease or ...
An equivalent type of Parkinson's disease developed in II-2 while II-1 showed no resting ... therefore, account for 13% of familial Parkinson's disease ...