Issue 3/2010
Content (10 Articles)
RNA processing pathways in amyotrophic lateral sclerosis
Marka van Blitterswijk, John E. Landers
Novel variants identified in methyl-CpG-binding domain genes in autistic individuals
Holly N. Cukier, Raquel Rabionet, Ioanna Konidari, Melissa Y. Rayner-Evans, Mary L. Baltos, Harry H. Wright, Ruth K. Abramson, Eden R. Martin, Michael L. Cuccaro, Margaret A. Pericak-Vance, John R. Gilbert
Analysis of exon dosage using MLPA in South African Parkinson's disease patients
Rowena J. Keyser, Debbie Lombard, Rene Veikondis, Jonathan Carr, Soraya Bardien
Hereditary spastic paraplegia and amyotrophy associated with a novel locus on chromosome 19
K. G. Meilleur, M. Traoré, M. Sangaré, A. Britton, G. Landouré, S. Coulibaly, B. Niaré, F. Mochel, A. La Pean, I. Rafferty, C. Watts, D. Shriner, M. T. Littleton-Kearney, C. Blackstone, A. Singleton, K. H. Fischbeck
Novel VLDLR microdeletion identified in two Turkish siblings with pachygyria and pontocerebellar atrophy
Luis E. Kolb, Zulfikar Arlier, Cengiz Yalcinkaya, Ali K. Ozturk, Jennifer A. Moliterno, Ozdem Erturk, Fatih Bayrakli, Baris Korkmaz, Michael L. DiLuna, Katsuhito Yasuno, Kaya Bilguvar, Tayfun Ozcelik, Beyhan Tuysuz, Matthew W. State, Murat Gunel
Meta-analysis of association between variation in the PDE4D gene and ischemic cerebral infarction risk in Asian populations
Xiaowei Xu, Xia Li, Jiejie Li, Ru Ou, Wenli Sheng
Fine mapping of the chromosome 10q11-q21 linkage region in Alzheimer's disease cases and controls
Margaret Daniele Fallin, Megan Szymanski, Ruihua Wang, Adrian Gherman, Susan S. Bassett, Dimitrios Avramopoulos
Molecular characterization of six Chinese families with m.3460G>A and Leber hereditary optic neuropathy
Dandan Yu, Xiaoyun Jia, A-Mei Zhang, Xiangming Guo, Ya-Ping Zhang, Qingjiong Zhang, Yong-Gang Yao
L239F founder mutation in GDAP1 is associated with a mild Charcot–Marie–Tooth type 4C4 (CMT4C4) phenotype
Dagmara Kabzińska, Halina Strugalska-Cynowska, Anna Kostera-Pruszczyk, Barbara Ryniewicz, Renata Posmyk, Alina Midro, Pavel Seeman, Lucia Báranková, Magdalena Zimoń, Jonathan Baets, Vincent Timmerman, Velina Guergueltcheva, Ivailo Tournev, Stayko Sarafov, Peter De Jonghe, Albena Jordanova, Irena Hausmanowa-Petrusewicz, Andrzej Kochański
Questionable association between a monoamine oxidase A promoter polymorphism and sudden infant death syndrome
Michael Klintschar, Christian Heimbold