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X-inactivation patterns in carriers of X-linked myotubular myopathy.
Kristiansen M, Knudsen GP, Tanner SM, McEntagart M, Jungbluth H, Muntoni F, Sewry C, Gallati S, Ørstavik KH, Wallgren-Pettersson C. Kristiansen M, et al. Among authors: gallati s. Neuromuscul Disord. 2003 Aug;13(6):468-71. doi: 10.1016/s0960-8966(03)00067-1. Neuromuscul Disord. 2003. PMID: 12899873
Mutations in the tight-junction gene claudin 19 (CLDN19) are associated with renal magnesium wasting, renal failure, and severe ocular involvement.
Konrad M, Schaller A, Seelow D, Pandey AV, Waldegger S, Lesslauer A, Vitzthum H, Suzuki Y, Luk JM, Becker C, Schlingmann KP, Schmid M, Rodriguez-Soriano J, Ariceta G, Cano F, Enriquez R, Juppner H, Bakkaloglu SA, Hediger MA, Gallati S, Neuhauss SC, Nurnberg P, Weber S. Konrad M, et al. Among authors: gallati s. Am J Hum Genet. 2006 Nov;79(5):949-57. doi: 10.1086/508617. Epub 2006 Sep 19. Am J Hum Genet. 2006. PMID: 17033971 Free PMC article.
Exon 17 skipping in CLCN1 leads to recessive myotonia congenita.
Chen L, Schaerer M, Lu ZH, Lang D, Joncourt F, Weis J, Fritschi J, Kappeler L, Gallati S, Sigel E, Burgunder JM. Chen L, et al. Among authors: gallati s. Muscle Nerve. 2004 May;29(5):670-6. doi: 10.1002/mus.20005. Muscle Nerve. 2004. PMID: 15116370
97 results