Identification of a novel polymorphism in the fibronectin type II domain of the SEL1L gene and possible relation to the persistent hyperinsulinemic hypoglycemia of infancy.

Saltini, G; Proverbio, M C; Malferrari, G; Biagiotti, L; Boettcher, P; Dominici, R; Monferini, E; Lorenzini, E; Cattaneo, M; Antonello, D; Moore, P S; Zamproni, I; Viscardi, M; Chiumello, G; Biunno, I

Saltini, G; Proverbio, M C; Malferrari, G; Biagiotti, L; Boettcher, P; Dominici, R; Monferini, E; Lorenzini, E; Cattaneo, M; Antonello, D; Moore, P S; Zamproni, I; Viscardi, M; Chiumello, G; Biunno, I.

Affiliation

Saltini G; Centre for Bio-molecular Interdisciplinary Studies and Industrial applications, University of Milan, Italy.

Mutat Res ; 554(1-2): 159-63, 2004 Oct 04.

Article in En | MEDLINE | ID: mdl-15450414

Subject(s)

Congenital Hyperinsulinism/genetics; Fibronectins/genetics; Polymorphism, Genetic; Proteins/genetics; Amino Acid Sequence; Child, Preschool; Chromosomes, Human, Pair 14; Humans; Infant; Molecular Sequence Data; Proteins/chemistry

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Collection: 01-internacional Database: MEDLINE Main subject: Polymorphism, Genetic / Proteins / Fibronectins / Congenital Hyperinsulinism Type of study: Diagnostic_studies Limits: Child, preschool / Humans / Infant Language: En Journal: Mutat Res Year: 2004 Document type: Article

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