... 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 ...

... 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 ...

... have an identified variant in any of these three genes. The cause of the disorder in these individuals is unknown. DCC NTN1 RAD51 Congenital mirror movement disorder is inherited in an autosomal dominant pattern, which means one copy of the altered ...

... to have an autosomal dominant pattern of inheritance. Autosomal dominant inheritance suggests that one copy of an altered gene ... ClinicalTrials.gov ...