Abstract
Annals of the New York Academy of SciencesVolume 605, Issue 1 p. 215-229 Implications of Double Mutant Phenotypesa SUSAN BILLINGS-GAGLIARDI, SUSAN BILLINGS-GAGLIARDI Department of Cell Biology University of Massachusetts Medical School Worcester, Massachusetts 01655Search for more papers by this authorMERRILL K. WOLF, MERRILL K. WOLF Department of Cell Biology University of Massachusetts Medical School Worcester, Massachusetts 01655Search for more papers by this author SUSAN BILLINGS-GAGLIARDI, SUSAN BILLINGS-GAGLIARDI Department of Cell Biology University of Massachusetts Medical School Worcester, Massachusetts 01655Search for more papers by this authorMERRILL K. WOLF, MERRILL K. WOLF Department of Cell Biology University of Massachusetts Medical School Worcester, Massachusetts 01655Search for more papers by this author First published: November 1990 https://doi.org/10.1111/j.1749-6632.1990.tb42394.xCitations: 3 a This work was supported by NIH Grant #NS 11425 (Javits Award). b In the interest of legibility we have simplified formal genetic notation as follows: shimld to mld and jpmsd to msd. AboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Citing Literature Volume605, Issue1Myelination and DysmyelinationNovember 1990Pages 215-229 RelatedInformation
Published Version
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a call