Open AccessComplex I respiratory defect in LHON plus dystonia with no mitochondrial DNA mutation
Author(s) -
Khaled K. AbuAmero,
Thomas M. Bosley,
Saeed Bohlega,
D. W. McLean
Publication year - 2005
Publication title -
british journal of ophthalmology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.016
H-Index - 153
eISSN - 1468-2079
pISSN - 0007-1161
DOI - 10.1136/bjo.2005.072819
Subject(s) - medicine , leber's hereditary optic neuropathy , ophthalmology , mitochondrial dna , abnormality , optic neuropathy , atrophy , nystagmus , anatomy , optic nerve , pathology , audiology , genetics , psychiatry , biology , gene
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom