Aix-Marseille University-ko ikertzaileekin lankidetzan egindako argitalpenak (2)

2014

  1. Entire CAPN3 gene deletion in a patient with limb-girdle muscular dystrophy type 2A

    Muscle and Nerve, Vol. 50, Núm. 3, pp. 448-453

2011

  1. Eosinophilic infiltration related to CAPN3 mutations: A pathophysiological component of primary calpainopathy?

    Clinical Genetics