intraflagellar transport protein 88 homolog isoform X8 [Homo sapiens]

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Ciliary Localization of the Intraflagellar Transport Protein IFT88 Is Disrupted in Cystic Fibrosis. [Am J Respir Cell Mol Biol. 2020]
Ciliary Localization of the Intraflagellar Transport Protein IFT88 Is Disrupted in Cystic Fibrosis.
Stevens EM, Vladar EK, Alanin MC, Christensen ST, von Buchwald C, Milla C. Am J Respir Cell Mol Biol. 2020 Jan; 62(1):120-123.
Association of IFT88 gene variants with nonsyndromic cleft lip with or without cleft palate. [Birth Defects Res. 2019]
Association of IFT88 gene variants with nonsyndromic cleft lip with or without cleft palate.
Barba A, Urbina C, Maili L, Greives MR, Blackwell SJ, Mulliken JB, Chiquet B, Blanton SH, Hecht JT, Letra A. Birth Defects Res. 2019 Jul 1; 111(11):659-665. Epub 2019 Apr 5.
IFT88 mutations identified in individuals with non-syndromic recessive retinal degeneration result in abnormal ciliogenesis. [Hum Genet. 2018]
IFT88 mutations identified in individuals with non-syndromic recessive retinal degeneration result in abnormal ciliogenesis.
Chekuri A, Guru AA, Biswas P, Branham K, Borooah S, Soto-Hermida A, Hicks M, Khan NW, Matsui H, Alapati A, et al. Hum Genet. 2018 Jul; 137(6-7):447-458. Epub 2018 Jul 5.

RefSeq protein isoforms
See 86 reference sequence protein isoforms for the IFT88 gene.

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Protein