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  • Identification and verification of novel disease-causing genes and therapy options for patients with mitochondrial disorders – focus on ACAD9 = Identifizierung und Verifizierung neuartiger krankheitsverursachender Gene und Therapiemöglichkeiten für Patienten mit mitochondrialen Erkrankungen - Fokus auf ACAD9 : [Dissertation]
    Haberberger, Birgit Monika
    Complex I deficiency is the most frequent mitochondrial disorder in childhood, characterized by marked clinical and genetic heterogeneity. In this work Whole-Exome Sequencing coupled with functional ... validation of new disease alleles, was successfully used in the identification of disease-causative variants in new and known complex I associated disease genes. The clinical, biochemical, and genetic spectrum of 70 patients with mutations in ACAD9, a complex I assembly factor, were analyzed in detail and in vitro analysis of patient-derived fibroblasts support bezafibrate and riboflavin as promising treatment options
    Vrsta gradiva - disertacija ; neleposlovje za odrasle
    Založništvo in izdelava - München : [B. M. Repp], 2019
    Jezik - angleški
    COBISS.SI-ID - 138540291

Nobena knjižnica v sistemu COBISS.SI nima izvoda tega gradiva (gre za elektronski vir ali pa poleg tiskane verzije obstaja tudi elektronska).
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