Coriell Logo
 
 Welcome Guest  
Current Location: Home > Publication Samples
Catalog Tools: 

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 YR567probandLEBER OPTIC ATROPHY
GM03858Male33 YR567probandLEBER OPTIC ATROPHY
GM10744Male53 YR1252probandLEBER OPTIC ATROPHY
GM10742Male30 YR probandLEBER OPTIC ATROPHY

  Support  
Skip Navigation Links.
     

Contact Us   |   Collections   |   Services   |   Feedback

© 2009 Coriell Institute. All rights reserved.
ISO:9001 Certified UL-DQS 10012308 QM08