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IFT88 mutations identified in individuals with non-syndromic recessive retinal degeneration result in abnormal ciliogenesis

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
Human Genetics · Vol. 137, Issue 6-7 · pp. 447-458 · 2018
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Bibliographic Information

JournalHuman Genetics
PublisherSpringer
Publication Date2018-07-01
Publication Year2018
Volume137
Issue6-7
Pages447-458
Document TypeJournal Article
Print ISSN0340-6717
eISSN1432-1203
DOI10.1007/s00439-018-1897-9

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NARA Access Coverage1964-01-01~Current
Journal Homepagehttps://www.springer.com/journal/439
Publisher PageOpen Publisher Page
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