Mutation screening in exons 3 and 4 of α-synuclein in sporadic Parkinson's and sporadic and familial dementia with Lewy bodies cases

NeuroReport

Volumn 9, Issue 17, 1998, Pages 3925-3927

  El Agnaf, Omar M A ^a,b   Curran, Martin D ^b   Wallace, Andrew ^a   Middleton, Derek ^a,b   Murgatroyd, Christopher ^c,d   Curtis, Anne ^c   Perry, Robert ^d   Jaros, Evelyn ^d  

^a QUEEN'S UNIVERSITY BELFAST   (United Kingdom)

^b BELFAST CITY HOSPITAL   (United Kingdom)

^c NEWCASTLE UNIVERSITY   (United Kingdom)

^d NEWCASTLE GENERAL HOSPITAL   (United Kingdom)

Author keywords

DNA sequencing; Familial dementia with Lewy body; Parkinson's disease; Synuclein mutations

Indexed keywords

ALPHA SYNUCLEIN;

ARTICLE; CONTROLLED STUDY; DEMENTIA; DNA SEQUENCE; FEMALE; GENETIC LINKAGE; GENETIC SCREENING; HUMAN; HUMAN CELL; HUMAN TISSUE; LEWY BODY; MAJOR CLINICAL STUDY; MALE; MISSENSE MUTATION; NUCLEOTIDE SEQUENCE; PARKINSON DISEASE; PRIORITY JOURNAL; SINGLE STRAND CONFORMATION POLYMORPHISM;

EID: 0032411220     PISSN: 09594965     EISSN: None     Source Type: Journal    
DOI: 10.1097/00001756-199812010-00029     Document Type: Article

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