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Parkinson disease "3," autosomal dominant
- ... 18, autosomal dominant, susceptibility to Genetic Testing Registry: Parkinson disease 3, autosomal dominant Genetic Testing Registry: Parkinson disease 5, autosomal dominant, ...
- ... Network. A frequent LRRK2 gene mutation associated with autosomal dominant Parkinson's disease. Lancet. 2005 Jan 29-Feb 4;365(9457): ...
- ... unclear why the signs and symptoms of this disease are related primarily to the frontal and temporal lobes. ... Chromosome 3-linked frontotemporal dementia DTM1 FTD-3 FTD-CHMP2B ...
- ... autosomal recessive Genetic Testing Registry: Visceral neuropathy, familial, 3, autosomal dominant Genetic Testing Registry: Intestinal pseudoobstruction, neuronal, chronic idiopathic, ...
- ... article on PubMed Central Kimonis VE, Watts GD. Autosomal dominant inclusion body myopathy, Paget disease of bone, and frontotemporal dementia. Alzheimer Dis Assoc ...
- Spinocerebellar Ataxias Including Machado-Joseph Disease (National Institute of Neurological Disorders and Stroke)Cerebellar Disorders/Specifics ... Cerebellar Disorders ... National Institute of Neurological Disorders and Stroke ... From the National Institutes of Health ... Spinocerebellar ...
- ... as sporadic and are not inherited.Familial Wolff-Parkinson-White syndrome accounts for only a small percentage of all cases of this condition. The familial form of the disorder typically has an autosomal dominant pattern of inheritance, which means one copy of ...
- ... to have an autosomal dominant pattern of inheritance. Autosomal dominant inheritance suggests that one copy of an altered gene ... ClinicalTrials.gov ...
- Dementias (National Institute of Neurological Disorders and Stroke)Dementia/Start Here ... Dementia ... Lewy Body Dementia/Statistics and Research ... Lewy Body Dementia ... National Institute of Neurological Disorders and Stroke ... From the ...
- ... essential tremor appears to be inherited in an autosomal dominant pattern, which means one copy of an altered ...