Condition: PARKINSON DISEASE 1, AUTOSOMAL DOMINANT (disorder)
rs104893875 in
SNCA gene and
PARKINSON DISEASE 1, AUTOSOMAL DOMINANT (disorder)
PMID 9197268 1997 Mutation in the alpha-synuclein gene identified in families with Parkinson's disease.
PMID 24936070 2014 The H50Q mutation enhances α-synuclein aggregation, secretion, and toxicity.
PMID 23457019 2013 Alpha-synuclein p.H50Q, a novel pathogenic mutation for Parkinson's disease.
PMID 14755719 2004 The new mutation, E46K, of alpha-synuclein causes Parkinson and Lewy body dementia.
PMID 23427326 2013 A novel α-synuclein missense mutation in Parkinson disease.
PMID 9462735 1998 Ala30Pro mutation in the gene encoding alpha-synuclein in Parkinson's disease.
PMID 25561023 2015 Molecular determinants of α-synuclein mutants' oligomerization and membrane interactions.
rs104893878 in
SNCA;SNCA-AS1 gene and
PARKINSON DISEASE 1, AUTOSOMAL DOMINANT (disorder)
PMID 23457019 2013 Alpha-synuclein p.H50Q, a novel pathogenic mutation for Parkinson's disease.
PMID 9462735 1998 Ala30Pro mutation in the gene encoding alpha-synuclein in Parkinson's disease.
PMID 9197268 1997 Mutation in the alpha-synuclein gene identified in families with Parkinson's disease.
PMID 23427326 2013 A novel α-synuclein missense mutation in Parkinson disease.
PMID 24936070 2014 The H50Q mutation enhances α-synuclein aggregation, secretion, and toxicity.
PMID 14755719 2004 The new mutation, E46K, of alpha-synuclein causes Parkinson and Lewy body dementia.
PMID 25561023 2015 Molecular determinants of α-synuclein mutants' oligomerization and membrane interactions.