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New POMT2 mutations causing congenital muscular dystrophy: identification of a founder mutation.

Akiko Yanagisawa , Céline Bouchet , Peter Y. K. van den Bergh , Jean-Marie Cuisset , Louis Viollet , et al.
Neurology, 2007, 69 (12), pp.1254-60. ⟨10.1212/01.wnl.0000268489.60809.c4⟩
Journal articles inserm-00201941v1

Les tests génétiques à l'heure de la deuxième révision des lois de bioéthique. [Genetic testing in the context of the revision of the French law on bioethics].

Dominique Bonneau , Sandrine Marlin , Damien Sanlaville , Jean-Michel Dupont , Hagay Sobol , et al.
Pathologie Biologie, 2010, 58 (5), pp.396-401. ⟨10.1016/j.patbio.2009.12.002⟩
Journal articles istex inserm-00461832v1

Use of SNP array analysis to identify a novel TRIM32 mutation in limb-girdle muscular dystrophy type 2H.

Mireille Cossée , Clotilde Lagier-Tourenne , Claire Seguela , Michel Mohr , France Leturcq , et al.
Neuromuscular Disorders, 2009, 19 (4), pp.255-60. ⟨10.1016/j.nmd.2009.02.003⟩
Journal articles istex inserm-00383333v1