SEMA3A, a gene involved in axonal pathfinding, is mutated in patients with Kallmann syndrome (Q34395316)

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SEMA3A, a gene involved in axonal pathfinding, is mutated in patients with Kallmann syndrome
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    SEMA3A, a gene involved in axonal pathfinding, is mutated in patients with Kallmann syndrome (English)
    Naresh Kumar Hanchate
    Pierre Lhuillier
    Jyoti Parkash
    Cécile Espy
    Corinne Fouveaut
    Chrystel Leroy
    Stéphanie Baron
    Céline Campagne
    Charlotte Vanacker
    Francis Collier
    Corinne Cruaud
    Vincent Meyer
    Alfons García-Piñero
    Didier Dewailly
    Ksenija Gersak
    Chantal Metz
    Gérard Chabrier
    Michel Pugeat
    Jacques Young
    Catherine Dodé
    23 August 2012
    e1002896

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