Novel missense, insertion and deletion mutations in the neurotrophic tyrosine kinase receptor type 1 gene (NTRK1) associated with congenital insensitivity to pain with anhidrosis (Q40432173)

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Novel missense, insertion and deletion mutations in the neurotrophic tyrosine kinase receptor type 1 gene (NTRK1) associated with congenital insensitivity to pain with anhidrosis
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    Novel missense, insertion and deletion mutations in the neurotrophic tyrosine kinase receptor type 1 gene (NTRK1) associated with congenital insensitivity to pain with anhidrosis (English)
    Kathrin Huehne
    Christiane Zweier
    Klaus Raab
    Sylvie Odent
    Martine Bonnaure-Mallet
    Jean-Louis Sixou
    Pierre Landrieu
    Cyril Goizet
    Jean Sarlangue
    Matthias Baumann
    Thomas Eggermann
    Sinje Ruppert
    Georg M Stettner
    Bernd Rautenstrauss
    20 February 2008
    159-166

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