A clinical, genetic, and neuropathologic study in a family with 16q-linked ADCA type III

Neurology

Volumn 65, Issue 4, 2005, Pages 629-632

  Owada, K ^a,e   Ishikawa, K ^a   Toru, S ^a   Ishida, G ^b   Gomyoda, M ^b   Tao, O ^a   Noguchi, Y ^a   Kitamura, K ^a   Kondo, I ^c   Noguchi, E ^d   Arinami, T ^d   Mizusawa, H ^a  

^a TOKYO MEDICAL AND DENTAL UNIVERSITY   (Japan)

^b National Hospital Organization   (Japan)

^c EHIME UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^d UNIVERSITY OF TSUKUBA   (Japan)

^e Department of Dermatology   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

CALBINDIN; DNA; UBIQUITIN;

ADOLESCENT; ADULT; AGED; ALLELE; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CASE REPORT; CEREBELLAR ATAXIA; CEREBELLUM ATROPHY; CHILD; CHROMOSOME 16Q; CLINICAL FEATURE; CONTROLLED STUDY; DISEASE ASSOCIATION; FAMILY STUDY; GENETIC LINKAGE; HAPLOTYPE; HEARING LOSS; HUMAN; HUMAN TISSUE; IMMUNOHISTOCHEMISTRY; INTERVIEW; NEUROLOGIC EXAMINATION; NEUROPATHOLOGY; NUCLEAR MAGNETIC RESONANCE IMAGING; PRIORITY JOURNAL;

EID: 23844449708     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/01.wnl.0000173065.75680.e2     Document Type: Article

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