MKS3/TMEM67 mutations are a major cause of COACH Syndrome, a Joubert Syndrome related disorder with liver involvement

Autor: Brancati, F., Iannicelli, M., Travaglini, L., Mazzotta, A., Bertini, E., Boltshauser, E., D?arrigo, S., Emma, F., Fazzi, E., Gallizzi, R., Gentile, M., Loncarevic, D., Mejaski-Bosnjak, V., Pantaleoni, C., Rigoli, L., Salpietro, C. D., Signorini, S., Stringini, G. R., Verloes, A., Zabloka, D., Dallapiccola, B., Gleeson, J. G., Valente, E. M., Zankl, A., Leventer, R., Smith, P. G., Janecke, A., D?hooghe, M., Sznajer, Y., Van Coster, R., Demerleir, L., Dias, K., Moco, C., Moreira, A., Ae Kim, C., Maegawa, G., Petkovic, D., Abdel-Salam, G. M. H., Abdel-Aleem, A., Zaki, M. S., Marti, I., Quijano-Roy, S., Sigaudy, S., De Lonlay, P., Romano, S., Touraine, R., Koenig, M., Lagier-Tourenne, C., Messer, J., Collignon, P., Wolf, N., Philippi, H., Tzeli, S. K., Halldorsson, S., Johannsdottir, J., Ludvigsson, P., Phadke, S. R., Udani, V., Stuart, B., Magee, A., Lev, D., Michelson, M., Ben-Zeev, B., Fischetto, R., Benedicenti, F., Stanzial, F., Borgatti, R., Accorsi, P., Battaglia, S., Giordano, L., Pinelli, L., Boccone, L., Bigoni, S., Ferlini, A., Donati, M. A., Caridi, G., Divizia, M. T., Faravelli, F., Ghiggeri, G., Pessagno, A., Briuglia, S., Tortorella, G., Adami, A., Castorina, P., Lalatta, F., Marra, G., Riva, D., Scelsa, B., Spaccini, L., Uziel, G., Giudice, E. D., Laverda, A. M., Ludwig, K., Permunian, A., Suppiej, A., Uggetti, C., Battini, R., Giacomo, M. D., Cilio, M. R., Di Sabato, M. L., Leuzzi, V., Parisi, P., Pollazzon, M., Silengo, M., De Vescovi, R., Greco, D., Romano, C., Cazzagon, M., Simonati, A., Al-Tawari, A. A., Bastaki, L., M('e)garban('e), A., Sabolic Avramovska, V., De Jong, M. M., Stromme, P., Koul, R., Rajab, A., Azam, M., Barbot, C., Martorell Sampol, L., Rodriguez, B., Pascual-Castroviejo, I., Teber, S., Anlar, B., Comu, S., Karaca, E., Kayserili, H., Y

Publikováno v: Human Mutation, 30(2), E432-E442. Wiley-Liss Inc.
International JSRD Study Group 2009, ' MKS3/TMEM67 mutations are a major cause of COACH syndrome, a joubert syndrome related disorder with liver involvement ', Human Mutation, vol. 30, no. 2, pp. E432-E442 . https://doi.org/10.1002/humu.20924

MKS3/TMEM67 mutations are a major cause of COACH Syndrome, a Joubert syndrome related disorder with liver involvement. The acronym COACH defines an autosomal recessive condition of Cerebellar vermis hypo/aplasia, Oligophrenia, congenital Ataxia, Colo

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5516a353ea15c6d875abcec34c7ef0e6
http://hdl.handle.net/11588/677358

A single human ciliopathy locus highlights the evolutionary dynamics of non-duplicated but adjacent genes

Autor: Lee, Jh, Silhavy, Jl, Lee, Je, Al Gazali, L, Thomas, S, Davis, Ee, Bielas, Sl, Hill, Kj, Gabriel, Sb, Brancati, F, Iannicelli, M, Russ, C, Logan, Cv, Sharif, Sm, Bennett, Cp, Abe, M, Hildebrandt, F, Diplas, Bh, Attié Bitach, T, Katsanis, N, Rajab, A, Koul, R, Sztriha, L, Waters, E, Ferro Novick, S, Woods, Gc, Johnson, Ca, Valente, Enza Maria, Zaki, Ms, Gleeson, J. G.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______3978::bbd833e8e6c81cb0c5dec78a01cf5133
http://hdl.handle.net/11570/1938202

Mutations in TMEM'16 perturb ciliogenesis and cause Joubert. Meckel and related syndromes

Autor: Valente, E. M., Logan, Cv, Mougou Zerelli, S., Lee, J. H., Silhavy, J. L., Brancati, F., Iannicelli, M., Travaglini, L., Romani, S., Illi, B., Adams, M., Szymanska, K., Mazzotta, A., Lee, J. E., Tolentino, J. C., Swistun, D., SALPIETRO DAMIANO, Carmelo, Fede, Carmelo Mario

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______3978::674ca2e7e89e0b62cb41207ae8773902
http://hdl.handle.net/11570/2325351

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