The COX8 gene is not the disease gene of the CMH4 locus in familial hypertrophic cardiomyopathy.

por Bonne, G, Carrier, L, Schwartz, K, Komajda, M
Publicado 1995

A new mutation of the lamin A/C gene leading to autosomal dominant axonal neuropathy, muscular dystrophy, cardiac disease, and leuconychia

por Goizet, C, Ben, Y, Demay, L, Richard, P, Bouillot, S, Rouanet, M, Hermosilla, E, Le Masson, G, Lagueny, A, Bonne, G, Ferrer, X
Publicado 2004

Lamin A N-terminal phosphorylation is associated with myoblast activation: impairment in Emery–Dreifuss muscular dystrophy

por Cenni, V, Sabatelli, P, Mattioli, E, Marmiroli, S, Capanni, C, Ognibene, A, Squarzoni, S, Maraldi, N, Bonne, G, Columbaro, M, Merlini, L, Lattanzi, G
Publicado 2005

First description of germline mosaicism in familial hypertrophic cardiomyopathy

por Forissier, J., Richard, P., Briault, S., Ledeuil, C., Dubourg, O., Charbonnier, B., Carrier, L., Moraine, C., Bonne, G., Komajda, M., Schwartz, K., Hainque, B.
Publicado 2000

Double heterozygosity for mutations in the β-myosin heavy chain and in the cardiac myosin binding protein C genes in a family with hypertrophic cardiomyopathy

por Richard, P., Isnard, R., Carrier, L., Dubourg, O., Donatien, Y., Mathieu, B., Bonne, G., Gary, F., Charron, P., Hagege, A., Komajda, M., Schwartz, K., Hainque, B.
Publicado 1999

Expanding the phenotype of LMNA mutations in dilated cardiomyopathy and functional consequences of these mutations

por Sebillon, P, Bouchier, C, Bidot, L, Bonne, G, Ahamed, K, Charron, P, Drouin-Garraud, V, Millaire, A, Desrumeaux, G, Benaiche, A, Charniot, J, Schwartz, K, Villard, E, Komajda, M
Publicado 2003