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Erschienen in: Journal of Neurology 3/2012

01.03.2012 | Letter to the Editors

Screening LRRK2 gene mutations in patients with Parkinson’s disease in Ghana

verfasst von: Roberto Cilia, Francesca Sironi, Albert Akpalu, Momodou Cham, Fred Stephen Sarfo, Tiziana Brambilla, Alba Bonetti, Marianna Amboni, Stefano Goldwurm, Gianni Pezzoli

Erschienen in: Journal of Neurology | Ausgabe 3/2012

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Dear Sirs, …
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Literatur
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Zurück zum Zitat Klein C, Schlossmacher MG (2006) The genetics of Parkinson disease: implications for neurological care. Nat Clin Pract Neurol 2:136–146PubMedCrossRef Klein C, Schlossmacher MG (2006) The genetics of Parkinson disease: implications for neurological care. Nat Clin Pract Neurol 2:136–146PubMedCrossRef
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Zurück zum Zitat Gilks WP, Abou-Sleiman PM, Gandhi S et al (2005) A common LRRK2 mutation in idiopathic Parkinson’s disease. Lancet 365:415–416PubMed Gilks WP, Abou-Sleiman PM, Gandhi S et al (2005) A common LRRK2 mutation in idiopathic Parkinson’s disease. Lancet 365:415–416PubMed
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Zurück zum Zitat Lesage S, Condroyer C, Lannuzel A et al (2009) Molecular analyses of the LRRK2 gene in European and North African autosomal dominant Parkinson’s disease. J Med Genet 46(7):458–464PubMedCrossRef Lesage S, Condroyer C, Lannuzel A et al (2009) Molecular analyses of the LRRK2 gene in European and North African autosomal dominant Parkinson’s disease. J Med Genet 46(7):458–464PubMedCrossRef
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Zurück zum Zitat Goldwurm S, Zini M, Mariani L et al (2007) Evaluation of LRRK2 G2019S penetrance: relevance for genetic counseling in Parkinson disease. Neurology 68(14):1141–1143PubMedCrossRef Goldwurm S, Zini M, Mariani L et al (2007) Evaluation of LRRK2 G2019S penetrance: relevance for genetic counseling in Parkinson disease. Neurology 68(14):1141–1143PubMedCrossRef
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Zurück zum Zitat Okubadejo N, Britton A, Crews C et al (2008) Analysis of Nigerians with apparently sporadic Parkinson disease for mutations in LRRK2, PRKN and ATXN3. PLoS One 3(10):e3421PubMedCrossRef Okubadejo N, Britton A, Crews C et al (2008) Analysis of Nigerians with apparently sporadic Parkinson disease for mutations in LRRK2, PRKN and ATXN3. PLoS One 3(10):e3421PubMedCrossRef
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Zurück zum Zitat Bardien S, Marsberg A, Keyser R et al (2010) LRRK2 G2019S mutation: frequency and haplotype data in South African Parkinson’s disease patients. J Neural Transm 117(7):847–853PubMedCrossRef Bardien S, Marsberg A, Keyser R et al (2010) LRRK2 G2019S mutation: frequency and haplotype data in South African Parkinson’s disease patients. J Neural Transm 117(7):847–853PubMedCrossRef
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Zurück zum Zitat Di Fonzo A, Rohe CF, Ferreira J et al (2005) A frequent LRRK2 gene mutation associated with autosomal dominant Parkinson’s disease. Lancet 365:412–415PubMedCrossRef Di Fonzo A, Rohe CF, Ferreira J et al (2005) A frequent LRRK2 gene mutation associated with autosomal dominant Parkinson’s disease. Lancet 365:412–415PubMedCrossRef
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Zurück zum Zitat Zabetian CP, Hutter CM, Yearout D et al (2006) LRRK2 G2019S in families with Parkinson disease who originated from Europe and the Middle East: evidence of two distinct founding events beginning two millennia ago. Am J Hum Genet 79(4):752–758PubMedCrossRef Zabetian CP, Hutter CM, Yearout D et al (2006) LRRK2 G2019S in families with Parkinson disease who originated from Europe and the Middle East: evidence of two distinct founding events beginning two millennia ago. Am J Hum Genet 79(4):752–758PubMedCrossRef
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Zurück zum Zitat Zabetian CP, Morino H, Ujike H et al (2006) Identification and haplotype analysis of LRRK2 G2019S in Japanese patients with Parkinson disease. Neurology 67(4):697–699PubMedCrossRef Zabetian CP, Morino H, Ujike H et al (2006) Identification and haplotype analysis of LRRK2 G2019S in Japanese patients with Parkinson disease. Neurology 67(4):697–699PubMedCrossRef
Metadaten
Titel
Screening LRRK2 gene mutations in patients with Parkinson’s disease in Ghana
verfasst von
Roberto Cilia
Francesca Sironi
Albert Akpalu
Momodou Cham
Fred Stephen Sarfo
Tiziana Brambilla
Alba Bonetti
Marianna Amboni
Stefano Goldwurm
Gianni Pezzoli
Publikationsdatum
01.03.2012
Verlag
Springer-Verlag
Erschienen in
Journal of Neurology / Ausgabe 3/2012
Print ISSN: 0340-5354
Elektronische ISSN: 1432-1459
DOI
https://doi.org/10.1007/s00415-011-6210-y

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