New parkin mutations and atypical phenotypes in families with autosomal recessive parkinsonism

Neurology

Volumn 60, Issue 8, 2003, Pages 1378-1381

  Rawal, N ^a   Periquet, M ^a   Lohmann, E ^a   Lucking C B ^b   Teive, H A ^c   Ambrosio, G ^d   Raskin, S ^e   Lincoln, S ^f   Hattori, N ^g   Guimaraes, J ^h   Horstink, M W I M ^l   Dos Santos Bele, W ⁱ   Brousolle, E ^j   Destee A ^k   Mizuno, Y ^g   Farrer, M ^f   Deleuze, J F ⁱ   De Michele, G ^d   Agid, Y ^a   Durr A ^a   Brice, Alexis ^a   more..

^a PITIÉ SALPÊTRIÈRE HOSPITAL   (France)

^b LUDWIG MAXIMILIANS UNIVERSITY   (Germany)

^c FEDERAL UNIVERSITY OF PARANÁ   (Brazil)

^d UNIVERSITY OF NAPLES FEDERICO II   (Italy)

^e Genetika   (Brazil)

^f Department of Neuroscience   (United States)

^g JUNTENDO UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^h HOSPITAL EGAS MONIZ   (Portugal)

ⁱ SANOFI   (France)

^j HOSPICES CIVILS DE LYON   (France)

^k LILLE UNIVERSITY HOSPITAL   (France)

^l CHRU de Lille ^*

more..

Author keywords

[No Author keywords available]

Indexed keywords

LEVODOPA;

ADULT; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; BIODIVERSITY; BRAZIL; CLINICAL ARTICLE; CONTROLLED STUDY; DISEASE COURSE; DISEASE SEVERITY; EUROPE; EVALUATION; FEMALE; GENE MUTATION; GEOGRAPHY; HUMAN; MALE; MUTATION RATE; ONSET AGE; PARKINSONISM; PHENOTYPE; PRIORITY JOURNAL; TREMOR;

EID: 0037461335     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/01.WNL.0000056167.89221.BE     Document Type: Article

References (10)

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3. Farrer M, Chan P, Chen R, et al. Lewy bodies and parkinsonism in families with parkin mutations. Ann Neurol 2001;50:293-300.
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8. Lücking CB, Brice A. Semiquantitative PCR for the detection of exon rearrangements in the parkin gene. In: Potter N. Methods in Molecular Medicine - Neurogenetics: Methods and Protocols. Totowa, NJ: Humana Press, 2003 (in press).
9. West A, Periquet M, Lincoln S, et al. Complex relationship between Parkin mutations and Parkinson disease. Am J Med Genet 2002;114:584-591.
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