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MBNL Sequestration by Toxic RNAs and RNA Misprocessing in the Myotonic Dystrophy Brain.
Goodwin M, Mohan A, Batra R, Lee KY, Charizanis K, Fernández Gómez FJ, Eddarkaoui S, Sergeant N, Buée L, Kimura T, Clark HB, Dalton J, Takamura K, Weyn-Vanhentenryck SM, Zhang C, Reid T, Ranum LP, Day JW, Swanson MS. Goodwin M, et al. Among authors: day jw. Cell Rep. 2015 Aug 18;12(7):1159-68. doi: 10.1016/j.celrep.2015.07.029. Epub 2015 Aug 6. Cell Rep. 2015. PMID: 26257173 Free PMC article.
Clinical and genetic characteristics of a five-generation family with a novel form of myotonic dystrophy (DM2).
Day JW, Roelofs R, Leroy B, Pech I, Benzow K, Ranum LP. Day JW, et al. Neuromuscul Disord. 1999 Jan;9(1):19-27. doi: 10.1016/s0960-8966(98)00094-7. Neuromuscul Disord. 1999. PMID: 10063831
We have recently mapped the disease locus (DM2) in this family to a 10 cM region of chromosome 3q [Ranum LPW, Rasmussen PF, Benzow KA, Koob MD, Day JW. Nat Genet 1998;19:196-198]. The genetically distinct form of myotonic dystrophy in the MN1 kindred shares some of …
We have recently mapped the disease locus (DM2) in this family to a 10 cM region of chromosome 3q [Ranum LPW, Rasmussen PF, Benzow KA, Koob …
213 results