Mitochondrial DNA Polymerase W748S Mutation: A Common Cause of Autosomal Recessive Ataxia with Ancient European Origin
The American Journal of Human Genetics2005Vol. 77(3), pp. 430–441
Citations Over TimeTop 10% of 2005 papers
Anna H. Hakonen, Silja Heiskanen, Vesa Juvonen, Ilse Lappalainen, Petri Luoma, Maria Rantamäki, Gert Van Goethem, A. Löfgren, Peter Hackman, Anders Paetau, Seppo Kaakkola, Kari Majamaa, Teppo Varilo, Bjarne Udd, Helena Kääriäinen, Laurence A. Bindoff, Anu Suomalainen
Related Papers
- → Evaluation of Cerebellar Ataxic Patients(2022)37 cited
- → Clinical features and haplotype analysis of newly identified Japanese patients with gelsolin-related familial amyloidosis of Finnish type(2012)17 cited
- → The western Swedish BRCA1 founder mutation 3171ins5; a 3.7 cM conserved haplotype of today is a reminiscence of a 1500-year-old mutation(2001)58 cited
- → Segawa syndrome due to mutation Q89X in the GCH1 gene: a possible founder effect in Córdoba (southern Spain)(2009)13 cited
- → Dutch myotonic dystrophy type 2 patients and a North-African DM2 family carry the common European founder haplotype(2011)8 cited