Mutations in IAPP and NEUROG3 genes are not a common cause of permanent neonatal/infancy/childhood-onset diabetes: Letter: Original Observations

Diabetic Medicine

Volumn 26, Issue 6, 2009, Pages 660-661

  Nocerino, V ^a   Colombo, C ^a   Bonfanti, R ^b   Iafusco, D ^c   Barbetti, F ^a,d  

^a BAMBINO GESÙ CHILDREN S HOSPITAL   (Italy)

^b SAN RAFFAELE HOSPITAL   (Italy)

^c SECOND UNIVERSITY OF NAPLES   (Italy)

^d UNIVERSITY OF ROME TOR VERGATA   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

AMYLIN; AUTOANTIBODY; GLUCAGON; GLUTAMATE DECARBOXYLASE; INSULIN; NEUROGENIN 3; PANCREAS ISLET CELL ANTIBODY; TRANSCRIPTION FACTOR; ZINC TRANSPORTER;

CHILDHOOD; DISEASE ASSOCIATION; DNA SEQUENCE; EXON; GENE EXPRESSION; GENE MUTATION; GROUPS BY AGE; HUMAN; INSULIN DEPENDENT DIABETES MELLITUS; INTRON; LETTER; NON INSULIN DEPENDENT DIABETES MELLITUS; ONSET AGE; PANCREAS ISLET BETA CELL;

AMYLOID; AUTOANTIBODIES; BASIC HELIX-LOOP-HELIX TRANSCRIPTION FACTORS; CHILD; CHILD, PRESCHOOL; DIABETES MELLITUS, TYPE 1; HUMANS; IMMUNOLOGIC FACTORS; INFANT; INFANT, NEWBORN; MUTATION; NERVE TISSUE PROTEINS;

EID: 66449133539     PISSN: 07423071     EISSN: 14645491     Source Type: Journal    
DOI: 10.1111/j.1464-5491.2009.02726.x     Document Type: Letter

References (12)

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