Latest Articles

Subject

Article
ABCA7 frameshift deletion associated with Alzheimer disease in African Americans
Holly N. Cukier, Brian W. Kunkle, Badri N. Vardarajan, et al.

May 17, 2016
Clinical/Scientific Notes
Homozygous GNAL mutation associated with familial childhood-onset generalized dystonia
Ikuo Masuho, Mingyan Fang, Chunyu Geng, et al.

May 12, 2016
Article
Screening for novel hexanucleotide repeat expansions at ALS- and FTD-associated loci
Fang He, Julie M. Jones, Claudia Figueroa-Romero, et al.

May 11, 2016
Clinical/Scientific Notes
White matter involvement in a family with a novel PDGFB mutation
Roberta Biancheri, Mariasavina Severino, Angela Robbiano, et al.

May 05, 2016
Article
Genomic mechanisms underlying PARK2 large deletions identified in a cohort of patients with PD
Sara Morais, Rita Bastos-Ferreira, Jorge Sequeiros, et al.

May 03, 2016
Clinical/Scientific Notes
FTL mutation in a Chinese pedigree with neuroferritinopathy
Wang Ni, Hong-Fu Li, Yi-Cen Zheng, et al.

April 27, 2016
Article
Parkinson disease (PARK) genes are somatically mutated in cutaneous melanoma
Rivka Inzelberg, Yardena Samuels, Esther Azizi, et al.

April 13, 2016
Article
Spinocerebellar ataxia type 36 in the Han Chinese
Yi-Chung Lee, Pei-Chien Tsai, Yuh-Cherng Guo, et al.

April 12, 2016
Article
DNA variants in CACNA1C modify Parkinson disease risk only when vitamin D level is deficient
Liyong Wang, Lizmarie Maldonado, Gary W. Beecham, et al.

April 12, 2016
Article
Clinical and genetic features of cervical dystonia in a large multicenter cohort
Mark S. LeDoux, Satya R. Vemula, Jianfeng Xiao, et al.

April 11, 2016

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