Complex relationship between Parkin mutations and Parkinson disease

American Journal of Medical Genetics - Neuropsychiatric Genetics

Volumn 114, Issue 5, 2002, Pages 584-591

  West, Andrew ^a   Periquet, Magali ^b   Lincoln, Sarah ^a   Lücking, Christoph B ^b,c   Nicholl, David ^d   Bonifati, Vincenzo ^e   Rawal, Nina ^b   Gasser, Thomas ^c   Lohmann, Ebba ^b   Deleuze, Jean François ^f   Maraganore, Demetrius ^g   Levey, Allan ^h   Wood, Nick ⁱ   Dürr, Alexandra ^b   Hardy, John ^a   Brice, Alexis ^b   Farrer, Matt ^a,j  

^a Department of Neuroscience   (United States)

^b INSERM   (France)

^c UNIVERSITY OF MUNICH   (Germany)

^d QUEEN ELIZABETH HOSPITAL   (United Kingdom)

^e SAPIENZA UNIVERSITY OF ROME   (Italy)

^f SANOFI   (France)

^g MAYO CLINIC   (United States)

^h EMORY UNIVERSITY SCHOOL OF MEDICINE   (United States)

ⁱ UNIVERSITY COLLEGE LONDON   (United Kingdom)

^j MAYO GRADUATE SCHOOL   (United States)

more..

Author keywords

Haplo insufficiency; Neurodegeneration; Parkin; Parkinson disease

Indexed keywords

PARKIN;

ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CLINICAL ARTICLE; EXON; GENE DELETION; GENE MUTATION; GENETIC SCREENING; HETEROZYGOSITY; HUMAN; INTRON; PARKINSON DISEASE; POINT MUTATION; PRIORITY JOURNAL; PROMOTER REGION;

ADOLESCENT; ADULT; ALLELES; ALTERNATIVE SPLICING; DNA; DNA MUTATIONAL ANALYSIS; EXONS; FEMALE; GENE FREQUENCY; GENOTYPE; HETEROZYGOTE; HUMANS; INTRONS; LIGASES; MALE; MIDDLE AGED; MUTATION; PARKINSON DISEASE; POLYMORPHISM, SINGLE NUCLEOTIDE; PROMOTER REGIONS (GENETICS); REVIEW LITERATURE; SEQUENCE DELETION; UBIQUITIN-PROTEIN LIGASES;

EID: 18444398035     PISSN: 15524841     EISSN: 1552485X     Source Type: Journal    
DOI: 10.1002/ajmg.10525     Document Type: Article

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