Distinctive features of degenerating Purkinje cells in spinocerebellar ataxia type 31

Abnormal RNA structures (RNA foci) containing a penta-nucleotide repeat (UGGAA)nin the Purkinje cell nucleus is associated with spinocerebellar ataxia type 31 pathogenesis

(2013) Yusuke Niimi et al.   NEUROPATHOLOGY

Spinocerebellar ataxia type 31 exists in Northeast China

(2012) Yi Ouyang et al.   JOURNAL OF THE NEUROLOGICAL SCIENCES

Pentanucleotide repeats at the spinocerebellar ataxia type 31 (SCA31) locus in Caucasians

(2011) K. Ishikawa et al.   NEUROLOGY

Analysis of an insertion mutation in a cohort of 94 patients with spinocerebellar ataxia type 31 from Nagano, Japan

(2010) Haruya Sakai et al.   NEUROGENETICS

SCA in Korea and its regional distribution: A multicenter analysis

(2010) Han-Joon Kim et al.   PARKINSONISM & RELATED DISORDERS

Spinocerebellar Ataxia Type 31 Is Associated with “Inserted” Penta-Nucleotide Repeats Containing (TGGAA)n

(2009) Nozomu Sato et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Golgi apparatus and neurodegenerative diseases

(2008) Jie Fan et al.   INTERNATIONAL JOURNAL OF DEVELOPMENTAL NEUROSCIENCE

Chromosome 16q22.1-linked autosomal dominant cerebellar ataxia: An autopsy case report with some new observations on cerebellar pathology

(2008) Masayuki Shintaku et al.   NEUROPATHOLOGY