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Dive into the research topics of 'IFT88 mutations identified in individuals with non-syndromic recessive retinal degeneration result in abnormal ciliogenesis'. Together they form a unique fingerprint.- Sort by
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Anil Chekuri, Aditya A. Guru, Pooja Biswas, Kari Branham, Shyamanga Borooah, Angel Soto-Hermida, Michael Hicks, Naheed W. Khan, Hiroko Matsui, Akhila Alapati, Pongali B. Raghavendra, Susanne Roosing, Sripriya Sarangapani, Sinnakaruppan Mathavan, Amalio Telenti, John R. Heckenlively, S. Amer Riazuddin, Kelly A. Frazer, Paul A. Sieving, Radha Ayyagari
Research output: Contribution to journal › Article › peer-review