Possible founder effect of rapsyn N88K mutation and identification of novel rapsyn mutations in congenital myasthenic syndromes

le Richard, P, Gaudon, K, Andreux, F, Yasaki, E, Prioleau, C, Bauche, S, Barois, A, Ioos, C, Mayer, M, Routon, M, Mokhtari, M, Leroy, J, Fournier, E, Hainque, B, Koenig, J, Fardeau, M, Eymard, B, Hantai, D
Foilsithe 2003

PCR based mutation screening of the laminin alpha2 chain gene (LAMA2): application to prenatal diagnosis and search for founder effects in congenital muscular dystrophy.

le Guicheney, P, Vignier, N, Zhang, X, He, Y, Cruaud, C, Frey, V, Helbling-Leclerc, A, Richard, P, Estournet, B, Merlini, L, Topaloglu, H, Mora, M, Harpey, J P, Haenggeli, C A, Barois, A, Hainque, B, Schwartz, K, Tomé, F M, Fardeau, M, Tryggvason, K
Foilsithe 1998