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Browsing by Author Brice, A.

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Showing results 2 to 7 of 7
Full TextIssue DateTitleAuthor(s)
2009Cerebellar Ataxia and Elevated Cerebrospinal Free Sialic AcidMochel, F.; Sedel, F.; Vanderver, A., et al
2009Cerebellar ataxia with elevated cerebrospinal free sialic acid (CAFSA).Mochel, F.; Sedel, F.; Vanderver, A., et al
2011Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studiesNalls, M.A.; Plagnol, V.; Hernandez, D.G., et al
2006Spine deformities in Charcot-Marie-Tooth 4C caused by SH3TC2 gene mutations.Azzedine, H.; Ravise, N.; Verny, C., et al
2010Targeted next-generation sequencing of a 12.5 Mb homozygous region reveals ANO10 mutations in patients with autosomal-recessive cerebellar ataxia.Vermeer, S.; Hoischen, A.; Meijer, R.P., et al
2011A two-stage meta-analysis identifies several new loci for Parkinson's disease.Plagnol, V.; Nalls, M.A.; Bras, J.M., et al
Showing results 2 to 7 of 7

 

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