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Liu, D. IFT43 Gene. Encyclopedia. Available online: https://encyclopedia.pub/entry/4153 (accessed on 29 September 2026).
Liu D. IFT43 Gene. Encyclopedia. Available at: https://encyclopedia.pub/entry/4153. Accessed September 29, 2026.
Liu, Dean. "IFT43 Gene" Encyclopedia, https://encyclopedia.pub/entry/4153 (accessed September 29, 2026).
Liu, D. (2020, December 23). IFT43 Gene. In Encyclopedia. https://encyclopedia.pub/entry/4153
Liu, Dean. "IFT43 Gene." Encyclopedia. Web. 23 December, 2020.
IFT43 Gene
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This entry is adapted from the peer-reviewed paper https://medlineplus.gov/genetics/gene/ift43

Intraflagellar transport 43

genes

References

  1. Arts H, Knoers N. Cranioectodermal Dysplasia. 2013 Sep 12 [updated 2018 Apr12]. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K,Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University ofWashington, Seattle; 1993-2020. Available fromhttp://www.ncbi.nlm.nih.gov/books/NBK154653/
  2. Arts HH, Bongers EM, Mans DA, van Beersum SE, Oud MM, Bolat E, Spruijt L,Cornelissen EA, Schuurs-Hoeijmakers JH, de Leeuw N, Cormier-Daire V, Brunner HG, Knoers NV, Roepman R. C14ORF179 encoding IFT43 is mutated in Sensenbrennersyndrome. J Med Genet. 2011 Jun;48(6):390-5. doi: 10.1136/jmg.2011.088864.
  3. Liem KF Jr, Ashe A, He M, Satir P, Moran J, Beier D, Wicking C, Anderson KV.The IFT-A complex regulates Shh signaling through cilia structure and membraneprotein trafficking. J Cell Biol. 2012 Jun 11;197(6):789-800. doi:10.1083/jcb.201110049.
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Subjects: Genetics & Heredity
Contributor MDPI registered users' name will be linked to their SciProfiles pages. To register with us, please refer to https://encyclopedia.pub/register : Dean Liu
View Times: 624
Entry Collection: MedlinePlus
Revision: 1 time (View History)
Update Date: 23 Dec 2020
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