Hypoglycaemia following diabetes remission in patients with 6q24 methylation defects: expanding the clinical phenotype

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Veröffentlicht in:	Diabetologia 2013-01, Vol.56 (1), p.218-221
Hauptverfasser:	Flanagan, S. E., Mackay, D. J. G., Greeley, S. A. W., McDonald, T. J., Mericq, V., Hassing, J., Richmond, E. J., Martin, W. R., Acerini, C., Kaulfers, A. M., Flynn, D. P., Popovic, J., Sperling, M. A., Hussain, K., Ellard, S., Hattersley, A. T.
Format:	Artikel
Sprache:	eng
Schlagworte:	Biological and medical sciences Birth weight Chromosome Deletion Chromosome Duplication Chromosomes Chromosomes, Human, Pair 6 - genetics Diabetes Diabetes Mellitus - congenital Diabetes Mellitus - genetics Diabetes Mellitus - metabolism Diabetes Mellitus - physiopathology Diabetes. Impaired glucose tolerance DNA Methylation Endocrine pancreas. Apud cells (diseases) Endocrinology Endocrinopathies Etiopathogenesis. Screening. Investigations. Target tissue resistance Fathers Female Genotype & phenotype Human Physiology Humans Hypoglycemia Hypoglycemia - etiology Hypoglycemia - therapy Infant, Newborn Infant, Newborn, Diseases - genetics Infant, Newborn, Diseases - metabolism Infant, Newborn, Diseases - physiopathology Insulin Internal Medicine Male Medical sciences Medicine Medicine & Public Health Metabolic Diseases Mutation Patients Remission (Medicine) Remission, Spontaneous Research Letter Uniparental Disomy
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