Reactome | Defects in the IFT-B component IFT172 cause Jeune and Mainzer-Saldino syndromes in humans

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Defects in the IFT-B component IFT172 cause Jeune and Mainzer-Saldino syndromes in humans Show undefined attributes

author	[Person:5617721] Halbritter, J [Person:5617712] Bizet, AA [Person:5617711] Schmidts, M [Person:5617708] Porath, JD [Person:5617717] Braun, DA [Person:5617704] Gee, HY [Person:5617694] McInerney-Leo, AM [Person:5617715] Krug, P [Person:5617698] Filhol, E [Person:5617517] Davis, EE [Person:5617725] Airik, R [Person:5617723] Czarnecki, PG [Person:5617716] Lehman, AM [Person:5617719] Trnka, P [Person:5617720] Nitschk�, P [Person:5420859] Bole-Feysot, C [Person:5617703] Schueler, M [Person:5617695] Knebelmann, B [Person:5617696] Burtey, S [Person:5617697] Szab�, AJ [Person:5617705] Tory, K [Person:5617707] Leo, PJ [Person:5617724] Gardiner, B [Person:5617699] McKenzie, FA [Person:2426283] Zankl, A [Person:5226936] Brown, MA [Person:5617709] Hartley, JL [Person:2471669] Maher, ER [Person:5617523] Li, C [Person:5617519] Leroux, MR [Person:5617701] Scambler, PJ [Person:5617714] Zhan, SH [Person:5617718] Jones, SJ [Person:2485027] Kayserili, H [Person:5617702] Tuysuz, B [Person:5617710] Moorani, KN [Person:5617713] Constantinescu, A [Person:2537592] Krantz, ID [Person:5617700] Kaplan, BS [Person:5610297] Shah, JV
created	[InstanceEdit:5617706] Rothfels, Karen, 2014-08-14
dbId	5617722
displayName	Defects in the IFT-B component IFT172 cause Jeune and Mainzer-Saldino syndromes in humans
journal	Am. J. Hum. Genet.
pages	915-25
pubMedIdentifier	24140113
schemaClass	LiteratureReference
title	Defects in the IFT-B component IFT172 cause Jeune and Mainzer-Saldino syndromes in humans
url	http://www.ncbi.nlm.nih.gov/pubmed/24140113
volume	93
year	2013

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[Reaction:R-HSA-5617820] Assembly of IFT B complex

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