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Springer Nature1
Journal
✓Human Genetics1
Publication Year
20181
S. Mathavan results 1 · Newest (Page 1/1, per page 25)
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Journal: Human Genetics ×Author: S. Mathavan ×Clear All Filters
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IFT88 mutations identified in individuals with non-syndromic recessive retinal degeneration result in abnormal ciliogenesisNARA Subscribed
Human Genetics · 2018 · Vol. 137 · Issue 6-7 · Springer
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
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