Fine Mapping and Identifying the Mutation Gene of Snthr-1 Bao Scant Hair Mouse
July 2009
in “
TSpace
”
Studysummary This study identified a 14,883 bp genomic deletion affecting the Plcd1 and Vill genes as likely responsible for the abnormal phenotype observed in snthr-1Bao mice.
Automatically generated from the study's abstract, not written by a person, and not a review of the full paper. Not medical advice or a treatment recommendation. Read the original study, and consult a qualified healthcare professional before changing treatment. Full disclaimer