This phenotypic mutation was identified in an ENU mutagenesis screen and shown to be an allele of Spnb4 by complementation testing versus the lumbosacral neuroaxonal dystrophy mutation of this gene. (J:82238)
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This phenotypic mutation was identified in an ENU mutagenesis screen and shown to be an allele of Spnb4 by complementation testing versus the lumbosacral neuroaxonal dystrophy mutation of this gene. (J:82238)