Search Results - Feener, C.A.

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  1. 1
    Cloning of Human Basic A1, a Distinct 59-kDa Dystrophin-Associated Protein Encoded on Chromosome 8q23-24

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

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  2. 2
    Primary γ-sarcoglycanopathy (LGMD 2C): broadening of the mutational spectrum guided by the immunohistochemical profile

    Primary γ-sarcoglycanopathy (LGMD 2C): broadening of the mutational spectrum guided by the immunohistochemical profile by 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.

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  3. 3
    Intrafamilial phenotypic variation in limb-girdle muscular dystrophy type 2C with compound heterozygous mutations

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

    Published in Muscle & nerve
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