IFT88 mutations identified in individuals with...

Human Genetics 2018 / 7

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

Chekuri, Anil, Guru, Aditya A., Biswas, Pooja, Branham, Kari, Borooah, Shyamanga, Soto-Hermida, Angel, Hicks, Michael, Khan, Naheed W., Matsui, Hiroko, Alapati, Akhila, Raghavendra, Pongali B., Roosin
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Language:
english
Journal:
Human Genetics
DOI:
10.1007/s00439-018-1897-9
Date:
July, 2018
File:
PDF, 1.60 MB
english, 2018
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