SEQUENCE ENCODING MAMMALIAN SULFONYLUREA RECEPTOR AND METHOD OF DETECTING PERSISTENT HYPERINSULINEMIC HYPOGLYCEMIA OF INFANCY

The present invention is directed to a method of detecting persistent hyperinsulinemic hypoglycemia of infancy comprising obtaining a sample comprising patient nucleic acids from a patient tissue sample; amplifying sulfonylurea receptor specific nucleic acids from said patient nucleic acids to produ...

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Main Authors BRYAN, LYDIA, AGUILAR, COTE, GILBERT, J, NELSON, DANIEL, A, THOMAS, PAMELA, M, BRYAN, JOSEPH, GAGEL, ROBERT, F
Format Patent
LanguageEnglish
French
German
Published 20.08.1997
Edition6
Subjects
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Summary:The present invention is directed to a method of detecting persistent hyperinsulinemic hypoglycemia of infancy comprising obtaining a sample comprising patient nucleic acids from a patient tissue sample; amplifying sulfonylurea receptor specific nucleic acids from said patient nucleic acids to produce a test fragment; obtaining a sample comprising control nucleic acids from a control tissue sample; amplifying control nucleic acids encoding wild type sulfonylurea receptor to produce a control fragment; comparing the test fragment with the control fragment to detect the presence of a sequence difference in the test fragment, wherein a difference in said test fragment indicates persistent hyperinsulinemic hypoglycemia of infancy. A diagnostic kit and primers for the detection of persistent hyperinsulinemic hypoglycemia of infancy are also within the scope of the present invention.
Bibliography:Application Number: EP19950916316