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Volumn 55, Issue 3, 2000, Pages 392-397

Hereditary motor and sensory neuropathy with myelin folding and juvenile onset glaucoma

Author keywords

[No Author keywords available]

Indexed keywords

MYELIN;

EID: 0033838030     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/WNL.55.3.392     Document Type: Article
Times cited : (23)

References (34)
  • 3
    • 0030900182 scopus 로고    scopus 로고
    • A clinical, electro-physiological, neuropathological, and genetic study of two Algerian families with an autosomal recessive demyelinating form of Chariot-Marie-Tooth disease
    • (1997) Neurology , vol.48 , pp. 867-873
    • Kessali, M.1    Zemmouri, R.2    Guilbot, A.3
  • 6
    • 0030015647 scopus 로고    scopus 로고
    • Localization of gene responsible for autosomal recessive demyelinating neuropathy with focally folded myelin sheaths to chromosome 11q23 by homozygosity mapping and haplotype sharing
    • (1996) Hum Mol Genet , vol.5 , pp. 1051-1054
    • Bolino, A.1    Brancolini, V.2    Bono, F.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.