The Tabby phenotype is caused by mutation in a mouse homologue of the EDA gene that reveals novel mouse and human exons and encodes a protein (ectodysplasin-A) with collagenous domains

A K Srivastava, J Pispa, A J Hartung, Y Z Du, S Ezer, T Jenks, T Shimada, M Pekkanen, M L Mikkola, M S H Ko, I Thesleff, J Kere, D Schlessinger

    Forskningsoutput: TidskriftsbidragArtikelVetenskapligPeer review

    Originalspråkengelska
    TidskriftProceedings of the National Academy of Sciences of the United States of America
    Volym94
    Sidor (från-till)13069-13074
    Antal sidor6
    ISSN0027-8424
    StatusPublicerad - 1997
    MoE-publikationstypA1 Tidskriftsartikel-refererad

    Vetenskapsgrenar

    • 311 Basmedicin

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    @article{7450e5e9893a441c8ffaa30cbd49b9e6,
    title = "The Tabby phenotype is caused by mutation in a mouse homologue of the EDA gene that reveals novel mouse and human exons and encodes a protein (ectodysplasin-A) with collagenous domains",
    keywords = "311 Basic medicine, geenit",
    author = "Srivastava, {A K} and J Pispa and Hartung, {A J} and Du, {Y Z} and S Ezer and T Jenks and T Shimada and M Pekkanen and Mikkola, {M L} and Ko, {M S H} and I Thesleff and J Kere and D Schlessinger",
    year = "1997",
    language = "English",
    volume = "94",
    pages = "13069--13074",
    journal = "Proceedings of the National Academy of Sciences of the United States of America",
    issn = "0027-8424",
    publisher = "National Academy of Sciences",

    }

    The Tabby phenotype is caused by mutation in a mouse homologue of the EDA gene that reveals novel mouse and human exons and encodes a protein (ectodysplasin-A) with collagenous domains. / Srivastava, A K ; Pispa, J ; Hartung, A J ; Du, Y Z ; Ezer, S ; Jenks, T ; Shimada, T ; Pekkanen, M ; Mikkola, M L ; Ko, M S H ; Thesleff, I ; Kere, J ; Schlessinger, D .

    I: Proceedings of the National Academy of Sciences of the United States of America, Vol. 94, 1997, s. 13069-13074.

    Forskningsoutput: TidskriftsbidragArtikelVetenskapligPeer review

    TY - JOUR

    T1 - The Tabby phenotype is caused by mutation in a mouse homologue of the EDA gene that reveals novel mouse and human exons and encodes a protein (ectodysplasin-A) with collagenous domains

    AU - Srivastava, A K

    AU - Pispa, J

    AU - Hartung, A J

    AU - Du, Y Z

    AU - Ezer, S

    AU - Jenks, T

    AU - Shimada, T

    AU - Pekkanen, M

    AU - Mikkola, M L

    AU - Ko, M S H

    AU - Thesleff, I

    AU - Kere, J

    AU - Schlessinger, D

    PY - 1997

    Y1 - 1997

    KW - 311 Basic medicine

    KW - geenit

    M3 - Article

    VL - 94

    SP - 13069

    EP - 13074

    JO - Proceedings of the National Academy of Sciences of the United States of America

    JF - Proceedings of the National Academy of Sciences of the United States of America

    SN - 0027-8424

    ER -