A new case of creatine transporter deficiency associated with mild clinical phenotype and a novel mutation in the SLC6A8 gene (Q43225506)

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scientific article published on 30 November 2009
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English
A new case of creatine transporter deficiency associated with mild clinical phenotype and a novel mutation in the SLC6A8 gene
scientific article published on 30 November 2009

    Statements

    A new case of creatine transporter deficiency associated with mild clinical phenotype and a novel mutation in the SLC6A8 gene (English)
    Patricia Alcaide
    Pilar Rodriguez-Pombo
    Pedro Ruiz-Sala
    Isaac Ferrer
    Pedro Castro
    Yolanda Ruiz Martin
    BegoƱa Merinero
    Magdalena Ugarte
    30 November 2009
    215-217

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