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Dive into the research topics of 'Identification of KIF21A mutations as a rare cause of congenital fibrosis of the extraocular muscles type 3 (CFEOM3)'. Together they form a unique fingerprint.- Sort by
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Koki Yamada, Wai Man Chan, Caroline Andrews, Thomas M. Bosley, Emin C. Sener, Johan T. Zwaan, Paul B. Mullaney, Banu T. Öztürk, A. Nurten Akarsu, Louise J. Sabol, Joseph L. Demer, Timothy J. Sullivan, Irene Gottlob, Peter Roggenkäemper, David A. Mackey, Clara E. De Uzcategui, Nicolas Uzcategui, Bruria Ben-Zeev, Elias I. Traboulsi, Adriano Magli
Research output: Contribution to journal › Article › peer-review