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Volumn 412, Issue 2, 1997, Pages 351-354

Mutations in subunit 6 of the F1F0-ATP synthase cause two entirely different diseases

Author keywords

F0; Leber hereditary optic neuropathy; Leber's disease; Mitochondrial disease; NARP syndrome; Proton translocation

Indexed keywords

MITOCHONDRIAL DNA; PROTON TRANSPORTING ADENOSINE TRIPHOSPHATE SYNTHASE;

EID: 0030753203     PISSN: 00145793     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0014-5793(97)00757-6     Document Type: Article
Times cited : (23)

References (25)


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.