Clinical Findings in a Large Family with a Parkin Ex3Δ40 Mutation

Archives of Neurology

Volumn 61, Issue 5, 2004, Pages 701-704

  Munhoz, Renato P ^a   Sa, Daniel S ^a   Rogaeva, Ekaterina ^b   Salehi Rad, Shabnam ^b   Sato, Christine ^b   Medeiros, Helena ^b   Farrer, Matthew ^c   Lang, Anthony E ^a  

^a UNIVERSITY OF TORONTO   (Canada)

^b UNIVERSITY OF TORONTO   (Canada)

^c MAYO GRADUATE SCHOOL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

FLUORINE 18; LEVODOPA;

ADULT; ARTICLE; AUTOSOMAL DOMINANT DISORDER; BASE PAIRING; CLINICAL FEATURE; CLINICAL GENETICS; DISEASE COURSE; ENVIRONMENTAL FACTOR; EXON; FAMILY; FEMALE; GENE; GENE DELETION; GENE MUTATION; GENETIC ANALYSIS; HETEROZYGOTE; HOMOZYGOSITY; HUMAN; MAJOR CLINICAL STUDY; MALE; NEUROPATHOLOGY; ONSET AGE; PARKIN GENE; PARKINSONISM; PATHOPHYSIOLOGY; POSITRON EMISSION TOMOGRAPHY; PRIORITY JOURNAL; RECESSIVE INHERITANCE; SYMPTOM;

ADULT; AGE OF ONSET; AGED; AGED, 80 AND OVER; DNA MUTATIONAL ANALYSIS; FEMALE; GENES, RECESSIVE; HUMANS; MALE; MIDDLE AGED; PARKINSONIAN DISORDERS; PEDIGREE; POINT MUTATION; POLYMERASE CHAIN REACTION; UBIQUITIN-PROTEIN LIGASES;

EID: 2442451698     PISSN: 00039942     EISSN: None     Source Type: Journal    
DOI: 10.1001/archneur.61.5.701     Document Type: Article

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