A spontaneous and novel Pax3 mutant mouse that models Waardenburg syndrome and neural tube defects.
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DOI: 10.1016/j.gene.2016.12.037
Abstract: BACKGROUND Genes responsible for reduced pigmentation phenotypes in rodents are associated with human developmental defects, such as Waardenburg syndrome, where patients display congenital deafness along with various abnormalities mostly related to neural crest development deficiency.… read more here.
Keywords: pax3; spontaneous novel; waardenburg syndrome; mutant mouse ... See more keywords