The Joubert-Meckel-Nephronophthisis Spectrum of Ciliopathies von Van De Weghe, Julie C, Gomez, Arianna, Doherty, Dan

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Protein transport in growing and steady‐state cilia von Lechtreck, Karl F., Van De Weghe, Julie C., Harris, James Aaron, Liu, Peiwei

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Super-resolution microscopy reveals that disruption of ciliary transition-zone architecture causes Joubert syndrome von Shi, Xiaoyu, Garcia, Galo, Van De Weghe, Julie C., McGorty, Ryan, Pazour, Gregory J., Doherty, Dan, Huang, Bo, Reiter, Jeremy F.

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TMEM218 dysfunction causes ciliopathies, including Joubert and Meckel syndromes von Van De Weghe, Julie C., Giordano, Jessica L., Mathijssen, Inge B., Mojarrad, Majid, Lugtenberg, Dorien, Miller, Caitlin V., Dempsey, Jennifer C., Mohajeri, Mahsa Sadat Asl, van Leeuwen, Elizabeth, Pajkrt, Eva, Klaver, Caroline C.W., Houlden, Henry, Eslahi, Atieh, Waters, Aoife M., Bamshad, Michael J., Nickerson, Deborah A., Aggarwal, Vimla S., de Vries, Bert B.A., Maroofian, Reza, Doherty, Dan

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Dysfunction of the ciliary ARMC9/TOGARAM1 protein module causes Joubert syndrome von Latour, Brooke L., Van de Weghe, Julie C., Rusterholz, Tamara D. S., Letteboer, Stef J. F., Gomez, Arianna, Shaheen, Ranad, Gesemann, Matthias, Karamzade, Arezou, Asadollahi, Mostafa, Barroso-Gil, Miguel, Chitre, Manali, Grout, Megan E., van Reeuwijk, Jeroen, van Beersum, Sylvia E. C., Miller, Caitlin, Dempsey, Jennifer C., Morsy, Heba, Bamshad, Michael J., Nickerson, Deborah A., Neuhauss, Stephan C. F., Boldt, Karsten, Ueffing, Marius, Keramatipour, Mohammad, Sayer, John A., Alkuraya, Fowzan S., Bachmann-Gagescu, Ruxandra, Roepman, Ronald, Doherty, Dan

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Mutations in ARMC9, which Encodes a Basal Body Protein, Cause Joubert Syndrome in Humans and Ciliopathy Phenotypes in Zebrafish von Van De Weghe, Julie C., Rusterholz, Tamara D.S., Latour, Brooke, Grout, Megan E., Aldinger, Kimberly A., Shaheen, Ranad, Dempsey, Jennifer C., Maddirevula, Sateesh, Cheng, Yong-Han H., Phelps, Ian G., Gesemann, Matthias, Goel, Himanshu, Birk, Ohad S., Alanzi, Talal, Rawashdeh, Rifaat, Khan, Arif O., Bamshad, Michael J., Nickerson, Deborah A., Neuhauss, Stephan C.F., Dobyns, William B., Alkuraya, Fowzan S., Roepman, Ronald, Bachmann-Gagescu, Ruxandra, Doherty, Dan

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Erratum: Super-resolution microscopy reveals that disruption of ciliary transition-zone architecture causes Joubert syndrome von Shi, Xiaoyu, Garcia, Galo, Van De Weghe, Julie C., McGorty, Ryan, Pazour, Gregory J., Doherty, Dan, Huang, Bo, Reiter, Jeremy F.

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Dysfunction of the ciliary ARMC9/TOGARAM1 protein module causes Joubert syndrome von Latour, Brooke L, Van De Weghe, Julie C, Rusterholz, Tamara D S, Letteboer, Stef J F, Gomez, Arianna, Shaheen, Ranad, Gesemann, Matthias, Karamzade, Arezou, Asadollahi, Mostafa, Barroso-Gil, Miguel, Chitre, Manali, Grout, Megan E, van Reeuwijk, Jeroen, van Beersum, Sylvia E C, Miller, Caitlin V, Dempsey, Jennifer C, Morsy, Heba, Bamshad, Michael J, Nickerson, Deborah A, Neuhauss, Stephan C F, Boldt, Karsten, Ueffing, Marius, Keramatipour, Mohammad, Sayer, John A, Alkuraya, Fowzan S, Bachmann-Gagescu, Ruxandra, Roepman, Ronald, Doherty, Dan

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Dysfunction of the ciliary ARMC9/TOGARAM1 protein module causes Joubert syndrome von Latour, Brooke L, Van De Weghe, Julie C, Rusterholz, Tamara D S, Letteboer, Stef J F, Gomez, Arianna, Shaheen, Ranad, Gesemann, Matthias, Karamzade, Arezou, Asadollahi, Mostafa, Barroso-Gil, Miguel, Chitre, Manali, Grout, Megan E, van Reeuwijk, Jeroen, van Beersum, Sylvia E C, Miller, Caitlin V, Dempsey, Jennifer C, Morsy, Heba, Bamshad, Michael J, Nickerson, Deborah A, Neuhauss, Stephan C F, Boldt, Karsten, Ueffing, Marius, Keramatipour, Mohammad, Sayer, John A, Alkuraya, Fowzan S, Bachmann-Gagescu, Ruxandra, Roepman, Ronald, Doherty, Dan

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Super-resolution microscopy reveals that disruption of ciliary transition zone architecture is a cause of Joubert syndrome von Shi, Xiaoyu, Garcia, Galo, Van De Weghe, Julie C., McGorty, Ryan, Pazour, Gregory J., Doherty, Dan, Huang, Bo, Reiter, Jeremy F.

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Mutations in ARMC9, which Encodes a Basal Body Protein, Cause Joubert Syndrome in Humans and Ciliopathy Phenotypes in Zebrafish von Van De Weghe, Julie C, Rusterholz, Tamara D S, Latour, Brooke, Grout, Megan E, Aldinger, Kimberly A, Shaheen, Ranad, Dempsey, Jennifer C, Maddirevula, Sateesh, Cheng, Yong-Han H, Phelps, Ian G, Gesemann, Matthias, Goel, Himanshu, Birk, Ohad S, Alanzi, Talal, Rawashdeh, Rifaat, Khan, Arif O, Bamshad, Michael J, Nickerson, Deborah A, Neuhauss, Stephan C F, Dobyns, William B, Alkuraya, Fowzan S, Roepman, Ronald, Bachmann-Gagescu, Ruxandra, Doherty, Dan

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ARMC9 and TOGARAM1 define a Joubert syndrome-associated protein module that regulates axonemal post-translational modifications and cilium stability von Latour, Brooke L, Van De Weghe, Julie C, Rusterholz, Tamara D S, Letteboer, Stef J F, Gomez, Arianna, Shaheen, Ranad, Gesemann, Matthias, Grout, Megan E, van Reeuwijk, Jeroen, van Beersum, Sylvia E C, Miller, Caitlin V, Dempsey, Jennifer C, Morsy, Heba, Bamshad, Michael J, Nickerson, Deborah A, Neuhauss, Stephan C F, Boldt, Karsten, Ueffing, Marius, Alkuraya, Fowzan S, Bachmann-Gagescu, Ruxandra, Roepman, Ronald, Doherty, Dan

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