Journal article
Use of transmitochondrial cybrids to assign a complex I defect to the mitochondrial DNA-encoded NADH dehydrogenase subunit 6 gene mutation at nucleotide pair 14459 that causes Leber hereditary optic neuropathy and dystonia
AS Jun, IA Trounce, MD Brown, JM Shoffner, DC Wallace
Molecular and Cellular Biology | AMER SOC MICROBIOLOGY | Published : 1996
DOI: 10.1128/mcb.16.3.771
Grants
Awarded by NHLBI NIH HHS
Awarded by NINDS NIH HHS