The recurrent mutation Arg258Gln in SYNJ1 (PARK20) is not a common cause of Parkinson's disease

Journal of Neurology

Volumn 261, Issue 4, 2014, Pages 833-834

  Winkler, Susen ^a   Vollstedt, Eva Juliane ^a   Kasten, Meike ^a   Alvarez Fischer, Daniel ^a   Klein, Christine ^a   Lohmann, Katja ^a  

^a UNIVERSITY OF LÜBECK   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ARGININE; GLYCINE; PARKIN; PHOSPHATASE; PHOSPHOINOSITIDE 5-PHOSPHATASE;

ADOLESCENT; ADULT; AGED; AMINO ACID SUBSTITUTION; CHILD; CONTROLLED STUDY; FAMILY HISTORY; FEMALE; GENE; GENE MUTATION; HUMAN; HUMAN CELL; LETTER; LYMPHOBLAST; MAJOR CLINICAL STUDY; MALE; MUTATIONAL ANALYSIS; PARKINSON DISEASE; PARKINSONISM; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM; SYNJ1 GENE; GENETICS; MIDDLE AGED; MUTATION; PHYSIOLOGY; VERY ELDERLY; YOUNG ADULT;

ADOLESCENT; ADULT; AGED; AGED, 80 AND OVER; CHILD; FEMALE; HUMANS; MALE; MIDDLE AGED; MUTATION; PARKINSON DISEASE; PHOSPHORIC MONOESTER HYDROLASES; YOUNG ADULT;

EID: 84898871589     PISSN: 03405354     EISSN: 14321459     Source Type: Journal    
DOI: 10.1007/s00415-014-7306-y     Document Type: Letter

References (6)

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