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Page 1
Multipoint mapping of the central core disease locus.
Schwemmle S, Wolff K, Palmucci LM, Grimm T, Lehmann-Horn F, Hübner C, Hauser E, Iles DE, MacLennan DH, Müller CR. Schwemmle S, et al. Among authors: palmucci lm. Genomics. 1993 Jul;17(1):205-7. doi: 10.1006/geno.1993.1302. Genomics. 1993. PMID: 8406450
Identification of four novel mutations in the C-terminal membrane spanning domain of the ryanodine receptor 1: association with central core disease and alteration of calcium homeostasis.
Tilgen N, Zorzato F, Halliger-Keller B, Muntoni F, Sewry C, Palmucci LM, Schneider C, Hauser E, Lehmann-Horn F, Müller CR, Treves S. Tilgen N, et al. Among authors: palmucci lm. Hum Mol Genet. 2001 Dec 1;10(25):2879-87. doi: 10.1093/hmg/10.25.2879. Hum Mol Genet. 2001. PMID: 11741831
Phenotypic clustering of lamin A/C mutations in neuromuscular patients.
Benedetti S, Menditto I, Degano M, Rodolico C, Merlini L, D'Amico A, Palmucci L, Berardinelli A, Pegoraro E, Trevisan CP, Morandi L, Moroni I, Galluzzi G, Bertini E, Toscano A, Olivè M, Bonne G, Mari F, Caldara R, Fazio R, Mammì I, Carrera P, Toniolo D, Comi G, Quattrini A, Ferrari M, Previtali SC. Benedetti S, et al. Neurology. 2007 Sep 18;69(12):1285-92. doi: 10.1212/01.wnl.0000261254.87181.80. Epub 2007 Mar 21. Neurology. 2007. PMID: 17377071