Publication

Wallace DC, Singh G, Lott MT, Hodge JA, Schurr TG, Lezza AM, Elsas LJ 2d, Nikoskelainen EK, Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy. Science242:1427-30 1988
PubMed ID: 3201231

Records Return:  (4) Show
 
Catalog IDGenderAge at SamplingFamilyRelationshipDescription
GM03857Male33 YR567probandCONGENITAL OPTIC ATROPHY, TYPE UNKNOWN
GM03858Male33 YR567probandCONGENITAL OPTIC ATROPHY, TYPE UNKNOWN
GM10744Male53 YR1252probandLEBER OPTIC ATROPHY
GM10742Male30 YR probandLEBER OPTIC ATROPHY