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Volumn 96, Issue 3, 1997, Pages 145-148

LHON mutations in Italian patients affected by multiple sclerosis

Author keywords

LHON; MS; mtDNA mutations

Indexed keywords

MITOCHONDRIAL DNA;

EID: 0030774591     PISSN: 00016314     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1600-0404.1997.tb00257.x     Document Type: Article
Times cited : (26)

References (26)
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    • in press
    • TORRONI A, PETROZZI M, D'URBANO L et al. Haplotype and phylogenetic analyses suggest that one European-specific mtDNA background plays a role in the expression of Leber hereditary optic neuropathy by increasing the penetrance of the primary mutations 11778 and 14484. Am J Hum Genet (1997, in press).
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.