A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe

Human Molecular Genetics

Volumn 8, Issue 4, 1999, Pages 567-574

  Abbas, Nacer ^a   Lücking, Christoph B ^a   Ricard, Sylvain ^b   Dürr, Alexandra ^a   Bonifati, Vincenzo ^c   De Michele, Giuseppe ^d   Bouley, Sandrine ^b   Vaughan, Jenny R ^e   Gasser, Thomas ^f   Marconi, Roberto ^g   Broussolle, Emmanuel ^h   Brefel Courbon, Christine ⁱ   Harhangi, Biswadjiet S ^j   Oostra, Ben A ^k   Fabrizio, Edito ^c   Böhme, Georg A ^b   Pradier, Laurent ^b   Wood, Nick W ^e   Filla, Alessandro ^d   Meco, Giuseppe ^c   Denefle, Patrice ^b   Agid, Yves ^a   Brice, Alexis ^a   more..

^a PITIÉ SALPÊTRIÈRE HOSPITAL   (France)

^b SANOFI   (France)

^c SAPIENZA UNIVERSITY OF ROME   (Italy)

^d UNIVERSITY OF NAPLES FEDERICO II   (Italy)

^e UNIVERSITY COLLEGE LONDON   (United Kingdom)

^f LUDWIG MAXIMILIANS UNIVERSITY   (Germany)

^g MISERICORDIA HOSPITAL   (Italy)

^h HÔPITAL NEUROLOGIQUE   (France)

ⁱ TOULOUSE UNIVERSITY HOSPITAL   (France)

^j ERASMUS MEDICAL CENTER   (Netherlands)

^k ERASMUS UNIVERSITY ROTTERDAM   (Netherlands)

more..

Author keywords

[No Author keywords available]

Indexed keywords

MUTANT PROTEIN; PARKIN; UNCLASSIFIED DRUG;

ARTICLE; AUTOSOMAL RECESSIVE DISORDER; EXON; FEMALE; FRAMESHIFT MUTATION; GENE MUTATION; HUMAN; HUMAN CELL; MALE; MISSENSE MUTATION; NONSENSE MUTATION; NUCLEOTIDE SEQUENCE; ONSET AGE; PARKINSONISM; PHENOTYPE; POINT MUTATION; PRIORITY JOURNAL;

EID: 0345490853     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/8.4.567     Document Type: Article

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