Senataxin mutations and amyotrophic lateral sclerosis

Genetic studies of amyotrophic lateral sclerosis: Controversies and perspectives

(2009) Ana Beleza-Meireles et al.   Amyotrophic Lateral Sclerosis

Ataxia with oculomotor apraxia type 2: clinical, biological and genotype/phenotype correlation study of a cohort of 90 patients

(2009) M. Anheim et al.   BRAIN

Ataxia oculomotor apraxia type 2: course over 27 years and a novel stop mutation in the senataxin gene

(2009) Tobias Haack et al.   JOURNAL OF NEUROLOGY

RNA processing defects associated with diseases of the motor neuron

(2009) Stephen J. Kolb et al.   MUSCLE & NERVE

Genetics of motor neuron disorders: new insights into pathogenic mechanisms

(2009) Patrick A. Dion et al.   NATURE REVIEWS GENETICS

A novel mutation in thesenataxingene identified in a Chinese patient with sporadic amyotrophic lateral sclerosis

(2008) Zhen-hua Zhao et al.   Amyotrophic Lateral Sclerosis

Identification and characterisation of a large Senataxin (SETX) gene duplication in ataxia with ocular apraxia type 2 (AOA2)

(2008) Larissa Arning et al.   NEUROGENETICS