Revista | Títol | Autors/es | | | BRAIN | Limb-girdle muscular dystrophy 1F is caused by a microdeletion in the transportin 3 gene. | Melia MJ, Kubota A, Ortolano S, Vilchez JJ, Gamez J, Tanji K, Bonilla E, Palenzuela L, Fernandez-Cad ... |  | | EXPERIMENTAL PHYSIOLOGY | Mitochondrial dysfunction and therapeutic approaches in respiratory and limb muscles of cancer cache ... | Fermoselle C, Garcia-Arumi E, Puig-Vilanova E, Andreu AL, Urtreger AJ, Bal de Kier Joffe ED, Tejedor ... | | | NEUROMUSCULAR DISORDERS | Identification of the novel mutation m.5658T>C in the mitochondrial tRNA(Asn) gene in a patient with ... | Pinos T, Melia MJ, Ortiz N, Martinez-Vea A, Raventos-Estelle A, Gallardo E, Hernandez-Losa J, Camara ... | | | Association of the K153R polymorphism in the myostatin gene and extreme longevity. | Garatachea N, Pinos T, Camara Y, Rodriguez-Romo G, Emanuele E, Ricevuti G, Venturini L, Santos-Lozan ... | | | Current Neurology and Neuroscience Reports | Neuromuscular disorders of glycogen metabolism. | Gazzerro E, Andreu AL, Bruno C | | | EUROPEAN JOURNAL OF CANCER | Hepatitis A virus cellular receptor 1/kidney injury molecule-1 is a susceptibility gene for clear ce ... | Cuadros T, Trilla E, Vila MR, de Torres I, Vilardell J, Messaoud NB, Salcedo M, Sarro E, Lopez-Helli ... | | |
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