Mutational analysis of the PINK1 gene in early-onset parkinsonism in Europe and North Africa

Brain

Volumn 129, Issue 3, 2006, Pages 686-694

  Ibáñez, Pablo ^a   Lesage, Suzanne ^a   Lohmann, Ebba ^a   Thobois, Stéphane ^b   De Michele, Giuseppe ^d   Borg, Michel ^c   Agid, Yves ^a   Dürr, Alexandra ^a   Brice, Alexis ^a  

^a PITIÉ SALPÊTRIÈRE HOSPITAL   (France)

^b HÔPITAL NEUROLOGIQUE   (France)

^c UNIVERSITY HOSPITAL OF NICE   (France)

^d UNIVERSITY OF NAPLES FEDERICO II   (Italy)

Author keywords

Early onset parkinsonism; Mutation; Parkin; PINK1

Indexed keywords

PARKIN; PHOSPHATIDYLINOSITOL 3,4,5 TRISPHOSPHATE 3 PHOSPHATASE;

ADULT; AGED; ARTICLE; CONTROLLED STUDY; DYSTONIA; EUROPE; FAMILY; FEMALE; GENE FREQUENCY; GENE MUTATION; GENETIC LINKAGE; GENETIC SCREENING; HETEROZYGOSITY; HOMOZYGOSITY; HUMAN; MAJOR CLINICAL STUDY; MALE; ONSET AGE; PARKINSON DISEASE; PATHOGENESIS; PRIORITY JOURNAL;

ADULT; AGE OF ONSET; AGED; AMINO ACID SEQUENCE; DNA MUTATIONAL ANALYSIS; FEMALE; HUMANS; MALE; MIDDLE AGED; MOLECULAR SEQUENCE DATA; MUTATION; PARKINSONIAN DISORDERS; PEDIGREE; PROTEIN KINASES; SEQUENCE ALIGNMENT; UBIQUITIN-PROTEIN LIGASES;

EID: 33244482539     PISSN: 00068950     EISSN: 14602156     Source Type: Journal    
DOI: 10.1093/brain/awl005     Document Type: Article

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