Functional analysis of three splicing mutations identified in the PMM2 gene: toward a new therapy for congenital disorder of glycosylation type Ia. (Q42612955)

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scientific article published on May 2009
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English
Functional analysis of three splicing mutations identified in the PMM2 gene: toward a new therapy for congenital disorder of glycosylation type Ia.
scientific article published on May 2009

    Statements

    Functional analysis of three splicing mutations identified in the PMM2 gene: toward a new therapy for congenital disorder of glycosylation type Ia. (English)
    Ana I Vega
    Celia Pérez-Cerdá
    Lourdes R Desviat
    Gert Matthijs
    Magdalena Ugarte
    Belén Pérez
    795-803

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