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

Mutation Research - Fundamental and Molecular Mechanisms of Mutagenesis

Volumn 554, Issue 1-2, 2004, Pages 159-163

  Saltini, G ^a   Proverbio, M C ^a   Malferrari, G ^a   Biagiotti, L ^a   Boettcher, P ^b   Dominici, R ^c   Monferini, E ^a   Lorenzini, E ^a   Cattaneo, M ^d   Antonello, D ^e   Moore, P S ^e   Zamproni, I ^f   Viscardi, M ^f   Chiumello, G ^f   Biunno, I ^a,d,g  

^a UNIVERSITY OF MILAN   (Italy)

^b Institute of Agricultural Biology and Biotechnology   (Italy)

^c UNIVERSITY OF MILAN   (Italy)

^d INSTITUTE OF BIOMEDICAL TECHNOLOGIES   (Italy)

^e UNIVERSITY OF VERONA   (Italy)

^f SAN RAFFAELE HOSPITAL   (Italy)

^g CNR   (Italy)

Author keywords

Fibronectin type II domain; SEL1L; SNP

Indexed keywords

FIBRONECTIN; FIBRONECTIN II; UNCLASSIFIED DRUG;

AMINO ACID COMPOSITION; ARTICLE; CONTROLLED STUDY; DISEASE ASSOCIATION; DNA POLYMORPHISM; EXON; GENE; GENE LOCATION; GENE MUTATION; GENETIC CODE; HUMAN; HUMAN TISSUE; HYPERINSULINEMIA; HYPOGLYCEMIA; INFANT DISEASE; MAJOR CLINICAL STUDY; NUCLEOTIDE SEQUENCE; PANCREAS TUMOR; PRIORITY JOURNAL; PROTEIN DOMAIN; SEL1L GENE;

AMINO ACID SEQUENCE; CHILD, PRESCHOOL; CHROMOSOMES, HUMAN, PAIR 14; FIBRONECTINS; HUMANS; INFANT; MOLECULAR SEQUENCE DATA; PERSISTENT HYPERINSULINEMIA HYPOGLYCEMIA OF INFANCY; POLYMORPHISM, GENETIC; PROTEINS;

EID: 4344693160     PISSN: 00275107     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.mrfmmm.2004.04.007     Document Type: Article

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