Reported mutations in GIGYF2 are not a common cause of Parkinson's disease

Movement Disorders

Volumn 24, Issue 4, 2009, Pages 619-620

  Vilariño Güell, Carles ^a   Ross, Owen A ^a   Soto, Alexandra I ^a   Farrer, Matthew J ^a   Haugarvoll, Kristoffer ^a,b   Aasly, Jan O ^c   Uitti, Ryan J ^a  

^a MAYO GRADUATE SCHOOL   (United States)

^b NORWEGIAN UNIVERSITY OF SCIENCE AND TECHNOLOGY   (Norway)

^c TRONDHEIM UNIVERSITY HOSPITAL   (Norway)

Author keywords

[No Author keywords available]

Indexed keywords

GENOMIC DNA; GROWTH FACTOR RECEPTOR BOUND PROTEIN 10 INTERACTING GYF PROTEIN 2; MEMBRANE PROTEIN; UNCLASSIFIED DRUG; CARRIER PROTEIN; GIGYF2 PROTEIN, HUMAN;

AMINO ACID SUBSTITUTION; CASE CONTROL STUDY; CASE REPORT; CAUCASIAN; CONTROLLED STUDY; DYSTONIA; ETHNICITY; FAMILY; GENDER; GENE MUTATION; GENE SEGREGATION; HUMAN; LETTER; MISSENSE MUTATION; NORWAY; ONSET AGE; PARKINSON DISEASE; PATHOGENICITY; PRIORITY JOURNAL; RESTLESS LEGS SYNDROME; SIBLING; UNITED STATES; AGED; COHORT ANALYSIS; FEMALE; GENETICS; MALE; MIDDLE AGED; MUTATION; NUCLEOTIDE SEQUENCE;

AGED; AGED, 80 AND OVER; CARRIER PROTEINS; COHORT STUDIES; DNA MUTATIONAL ANALYSIS; FEMALE; HUMANS; MALE; MIDDLE AGED; MUTATION; PARKINSON DISEASE; UNITED STATES;

EID: 64649086954     PISSN: 08853185     EISSN: 15318257     Source Type: Journal    
DOI: 10.1002/mds.22451     Document Type: Letter

References (4)

1. Farrer MJ. Genetics of Parkinson disease: paradigm shifts and future prospects. Nat Rev Genet 2006;7:306-318.
2. Lautier C, Goldwurm S, Durr A, et al. Mutations in the GIGYF2 (TNRC15) gene at the PARK11 locus in familial Parkinson disease. Am J Hum Genet 2008;82:822-833.
3. Pankratz N, Nichols WC, Uniacke SK, et al. Significant linkage of Parkinson disease to chromosome 2q36-37. Am J Hum Genet 2003;72:1053-1057.
4. Gelb DJ, Oliver E, Gilman S. Diagnostic criteria for Parkinson disease. Arch Neurol 1999;56:33-39.