Detection of AGXT bgene mutations by denaturing high-performance liquid chromatography for diagnosis of hyperoxaluria type 1.

Pirulli, D; Giordano, M; Lessi, M; Spanò, A; Puzzer, D; Zezlina, S; Boniotto, M; Crovella, S; Florian, F; Marangella, M; Momigliano-Richiardi, P; Savoldi, S; Amoroso, A

Pirulli, D; Giordano, M; Lessi, M; Spanò, A; Puzzer, D; Zezlina, S; Boniotto, M; Crovella, S; Florian, F; Marangella, M; Momigliano-Richiardi, P; Savoldi, S; Amoroso, A.

Affiliation

Pirulli D; Department of Sciences of Reproduction and Development, University of Trieste, Italy.

Clin Exp Med ; 1(2): 99-104, 2001 Jun.

Article in En | MEDLINE | ID: mdl-11699734

Subject(s)

Chromatography, High Pressure Liquid/methods; DNA Mutational Analysis/methods; Hyperoxaluria, Primary/diagnosis; Transaminases/genetics; Adolescent; Adult; Child; Child, Preschool; Female; Humans; Infant; Male; Middle Aged; Mutation; Polymerase Chain Reaction; Sensitivity and Specificity

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Collection: 01-internacional Database: MEDLINE Main subject: Hyperoxaluria, Primary / DNA Mutational Analysis / Chromatography, High Pressure Liquid / Transaminases Type of study: Clinical_trials / Diagnostic_studies / Prognostic_studies Limits: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male / Middle aged Language: En Journal: Clin Exp Med Year: 2001 Document type: Article

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