The mutation was identified as an A to C transversion causing a missense mutation that predicts a Thr5000Pro substitution in the rod 2b domain, a domain known to be important for keratin keratin interactions. (J:81301)
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The mutation was identified as an A to C transversion causing a missense mutation that predicts a Thr5000Pro substitution in the rod 2b domain, a domain known to be important for keratin keratin interactions. (J:81301)