Mutations in B9D1 and MKS1 cause mild Joubert syndrome: expanding the genetic overlap with the lethal ciliopathy Meckel syndrome (Q42752301)

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scientific article published on 5 May 2014
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Mutations in B9D1 and MKS1 cause mild Joubert syndrome: expanding the genetic overlap with the lethal ciliopathy Meckel syndrome
scientific article published on 5 May 2014

    Statements

    Mutations in B9D1 and MKS1 cause mild Joubert syndrome: expanding the genetic overlap with the lethal ciliopathy Meckel syndrome (English)
    Maria Teresa Dotti
    László Sztriha
    Francesca Mancini
    Benrhouma Hanene
    Maria Alessandra Carluccio
    Adrienn Máté
    Alíz Zimmermann
    Neziha Gouider-Khouja

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