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Dive into the research topics of 'The Noonan Syndrome-linked Raf1L613V mutation drives increased glial number in the mouse cortex and enhanced learning'. Together they form a unique fingerprint.- Sort by
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Michael C. Holter, Lauren T. Hewitt, Stephanie V. Koebele, Jessica M. Judd, Lei Xing, Heather A. Bimonte-Nelson, Cheryl D. Conrad, Toshiyuki Araki, Benjamin G. Neel, William D. Snider, Jason M. Newbern
Research output: Contribution to journal › Article › peer-review