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Compound heterozygosity in a South African patient with facioscapulohumeral muscular dystrophy.
Neuromuscul Disord. 2012 Aug;22(8):728-34. doi: 10.1016/j.nmd.2012.04.009. Epub 2012 May 29.
Neuromuscul Disord. 2012.
PMID: 22652079
Association of the calpain-10 gene with type 2 diabetes in Europeans: results of pooled and meta-analyses.
Tsuchiya T, Schwarz PE, Bosque-Plata LD, Geoffrey Hayes M, Dina C, Froguel P, Wayne Towers G, Fischer S, Temelkova-Kurktschiev T, Rietzsch H, Graessler J, Vcelák J, Palyzová D, Selisko T, Bendlová B, Schulze J, Julius U, Hanefeld M, Weedon MN, Evans JC, Frayling TM, Hattersley AT, Orho-Melander M, Groop L, Malecki MT, Hansen T, Pedersen O, Fingerlin TE, Boehnke M, Hanis CL, Cox NJ, Bell GI.
Tsuchiya T, et al. Among authors: wayne towers g.
Mol Genet Metab. 2006 Sep-Oct;89(1-2):174-84. doi: 10.1016/j.ymgme.2006.05.013. Epub 2006 Jul 11.
Mol Genet Metab. 2006.
PMID: 16837224
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