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Items: 2

    • Showing Current items.

    Name/Gene IDDescriptionLocationAliasesMIM
    ID: 7486
    Werner syndrome RecQ like helicase [Homo sapiens (human)]Chromosome 8, NC_000008.11 (31033262..31173761)RECQ3, RECQL2, RECQL3604611
    ID: 4312
    matrix metallopeptidase 1 [Homo sapiens (human)]Chromosome 11, NC_000011.10 (102789910..102798235, complement)CLG, CLGN120353
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