| http://www.w3.org/ns/prov#value | - The mutation is a C to T base change that results in a change of an arginine to an apparent premature stop codon at amino acid 108, and in all likelihood accounts for the 1J mutation (FIG. 14) despite high level expression of the ob mRNA (see FIG. 12 and FIG. 13, C57BL/6J ob/ob lanes).
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