Phenotypic spectrum of PINK1-associated Parkinsonism in 15 mutation carriers from 1 family

Movement Disorders

Volumn 22, Issue 1, 2007, Pages 145-147

  Hiller, Anja ^a   Hagenah, Johann M ^a   Djarmati, Ana ^a   Hedrich, Katja ^a   Reetz, Kathrin ^a   Schneider Gold, Christiane ^b   Kress, Wolfgang ^c   Münchau, Alexander ^d   Klein, Christine ^a  

^a UNIVERSITY OF LÜBECK   (Germany)

^b UNIVERSITY OF GÖTTINGEN   (Germany)

^c UNIVERSITY OF WÜRZBURG   (Germany)

^d UNIVERSITY OF HAMBURG   (Germany)

Author keywords

Mutation carriers; Phenotype; PINK1

Indexed keywords

CABERGOLINE; LEVODOPA; SELEGILINE;

ADULT; AGED; ARTICLE; CLINICAL ARTICLE; CLINICAL FEATURE; CONTROLLED STUDY; FEMALE; GENE; GENE MUTATION; HETEROZYGOTE; HUMAN; MALE; PARKINSONISM; PHENOTYPE; PINK1 GENE; PRIORITY JOURNAL;

ADULT; AGED; CARRIER STATE; DNA MUTATIONAL ANALYSIS; FAMILY HEALTH; FEMALE; GENETIC PREDISPOSITION TO DISEASE; HUMANS; MALE; MIDDLE AGED; MUTATION; PARKINSONIAN DISORDERS; PHENOTYPE; PROTEIN KINASES;

EID: 33847745843     PISSN: 08853185     EISSN: 15318257     Source Type: Journal    
DOI: 10.1002/mds.21059     Document Type: Article

References (6)

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