Reactome | Mutations in the cilia gene ARL13B lead to the classical form of Joubert syndrome

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Mutations in the cilia gene ARL13B lead to the classical form of Joubert syndrome Show undefined attributes

author	[Person:3621717] Cantagrel, V [Person:4420035] Silhavy, JL [Person:4420001] Bielas, SL [Person:4420031] Swistun, D [Person:5624714] Marsh, SE [Person:5624596] Bertrand, JY [Person:5624585] Audollent, S [Person:2453883] Atti�-Bitach, T [Person:5624655] Holden, KR [Person:4420023] Dobyns, WB [Person:5624776] Traver, D [Person:508046] Al-Gazali, L [Person:3621774] Ali, BR [Person:3621723] Lindner, TH [Person:5624610] Caspary, T [Person:5624724] Otto, EA [Person:5624658] Hildebrandt, F [Person:5624645] Glass, IA [Person:5624702] Logan, CV [Person:5624674] Johnson, CA [Person:5624593] Bennett, C [Person:508082] Brancati, F
created	[InstanceEdit:5624830] Rothfels, Karen, 2014-09-30
dbId	5624829
displayName	Mutations in the cilia gene ARL13B lead to the classical form of Joubert syndrome
journal	Am. J. Hum. Genet.
pages	170-9
pubMedIdentifier	18674751
schemaClass	LiteratureReference
title	Mutations in the cilia gene ARL13B lead to the classical form of Joubert syndrome
url	http://www.ncbi.nlm.nih.gov/pubmed/18674751
volume	83
year	2008

Referrals

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[Pathway:R-HSA-5624958] ARL13B-mediated ciliary trafficking of INPP5E

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