Cloning of Human Basic A1, a Distinct 59-kDa Dystrophin-Associated Protein Encoded on Chromosome 8q23-24 von Ahn, Andrew H., Yoshida, Mikiharu, Anderson, MaryDilys S., Feener, Chris A., Selig, Sara, Hagiwara, Yasuko, Ozawa, Eijiro, Kunkel, Louis M.

Volltext

Primary γ-sarcoglycanopathy (LGMD 2C): broadening of the mutational spectrum guided by the immunohistochemical profile von Bönnemann, C.G., Wong, J., Jones, K.J., Lidov, H.G.W., Feener, C.A., Shapiro, F., Darras, B.T., Kunkel, L.M., North, K.N.

Volltext

Intrafamilial phenotypic variation in limb-girdle muscular dystrophy type 2C with compound heterozygous mutations von Takano, A., Bönnemann, C.G., Honda, H., Sakai, M., Feener, C.A., Kunkel, L.M., Sobue, G.

Volltext

Cloning of Human Microtubule-Associated Protein 1B and the Identification of a Related Gene on Chromosome 15 von Lien, Lyndon L., Feener, Chris A., Fischbach, Neal, Kunkel, Louis M.

Volltext