EIF4G1 R1205H and VPS35 D620N mutations are rare in Parkinson's disease from South Africa

Neurobiology of Aging

Volumn 35, Issue 2, 2014, Pages 445.e1-445.e3

  Blanckenberg, Janine ^a   Ntsapi, Claudia ^a   Carr, Jonathan A ^a   Bardien, Soraya ^a  

^a UNIVERSITY OF STELLENBOSCH   (South Africa)

Author keywords

D620N mutation; EIF4G1 gene; Parkinson's disease; R1205H mutation; South Africa; VPS35 gene

Indexed keywords

AFRICA SOUTH OF THE SAHARA; ARTICLE; ASSAY; CONTROLLED STUDY; ETHNICITY; EUKARYOTIC TRANSLATION INITIATION FACTOR 4G1 GENE; GENE; GENE MUTATION; GENETIC SCREENING; GENOTYPE; HUMAN; MAJOR CLINICAL STUDY; MUTATION RATE; PARKINSON DISEASE; PRIORITY JOURNAL; SOUTH AFRICA; VACUOLAR PROTEIN SORTING 35 GENE;

D620N MUTATION; EIF4G1 GENE; PARKINSON'S DISEASE; R1205H MUTATION; SOUTH AFRICA; VPS35 GENE;

DISEASE SUSCEPTIBILITY; EUKARYOTIC INITIATION FACTOR-4G; GENOTYPING TECHNIQUES; HUMANS; MUTATION; MUTATION RATE; PARKINSONIAN DISORDERS; SOUTH AFRICA; VESICULAR TRANSPORT PROTEINS;

EID: 84887233439     PISSN: 01974580     EISSN: 15581497     Source Type: Journal    
DOI: 10.1016/j.neurobiolaging.2013.08.023     Document Type: Article

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