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Volumn 58, Issue 3, 2002, Pages 411-416

Spastic paraplegia, ataxia, mental retardation (SPAR): A novel genetic disorder

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; ATAXIA; CEREBELLUM ATROPHY; CLINICAL ARTICLE; DOMINANT INHERITANCE; ELECTROMYOGRAPHY; FAMILY STUDY; FEMALE; GENE LOCUS; GENE MUTATION; GENE SEGREGATION; GENETIC ANALYSIS; GENETIC DISORDER; GENETIC LINKAGE; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; MALE; MENTAL DEFICIENCY; NERVE CONDUCTION; NEUROLOGIC EXAMINATION; NUCLEAR MAGNETIC RESONANCE IMAGING; ONSET AGE; PHENOTYPE; PRIORITY JOURNAL; SPASTIC PARAPLEGIA; SPASTIC PARAPLEGIA ATAXIA MENTAL RETARDATION SYNDROME; SPINAL CORD ATROPHY; TRINUCLEOTIDE REPEAT;

EID: 0037065770     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/WNL.58.3.411     Document Type: Article
Times cited : (18)

References (23)
  • 3
  • 17
    • 0029959667 scopus 로고    scopus 로고
    • Autosomal dominant cerebellar ataxia type I: Clinical features and MRI in families with SCA1, SCA2, and SCA3
    • (1996) Brain , vol.119 , pp. 1497-1505
    • Burk, K.1    Abele, M.2    Fetter, M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.