Characterisation of new KATP-channel mutations associated with congenital hyperinsulinism in the Finnish population

Diabetologia

Volumn 46, Issue 2, 2003, Pages 241-249

  Reimann, F ^a   Huopio, H ^b   Dabrowski, M ^c   Proks, P ^c   Gribble, F M ^a   Laakso, M ^b   Otonkoski, T ^d   Ashcroft, F M ^c  

^a UNIVERSITY OF CAMBRIDGE   (United Kingdom)

^b KUOPIO UNIVERSITY HOSPITAL   (Finland)

^c UNIVERSITY OF OXFORD   (United Kingdom)

^d UNIVERSITY OF HELSINKI   (Finland)

Author keywords

ATP sensitive potassium channel; Congenital hyperinsulinism; Sulphonylurea receptor

Indexed keywords

ADENOSINE TRIPHOSPHATE; DIAZOXIDE; EPITOPE; MAGNESIUM DERIVATIVE; POTASSIUM CHANNEL; PROTEIN SUBUNIT; ABC TRANSPORTER; DRUG RECEPTOR; INWARDLY RECTIFYING POTASSIUM CHANNEL; SULFONYLUREA RECEPTOR;

ANIMAL CELL; ANIMAL EXPERIMENT; ARTICLE; CELL MEMBRANE; CONTROLLED STUDY; ENZYME LINKED IMMUNOSORBENT ASSAY; FEMALE; FINLAND; GENE MUTATION; HUMAN; HYPERINSULINISM; MOLECULAR BIOLOGY; NONHUMAN; NUCLEOTIDE SEQUENCE; OOCYTE; POPULATION RESEARCH; PRIORITY JOURNAL; PROTEIN EXPRESSION; WILD TYPE; XENOPUS LAEVIS; ANIMAL; ELECTRIC CONDUCTIVITY; GENETICS; METABOLISM; MUTATION; PHYSIOLOGY;

ANIMALS; ATP-BINDING CASSETTE TRANSPORTERS; CELL MEMBRANE; ELECTRIC CONDUCTIVITY; FEMALE; FINLAND; HUMANS; HYPERINSULINISM; MUTATION; OOCYTES; POTASSIUM CHANNELS; POTASSIUM CHANNELS, INWARDLY RECTIFYING; RECEPTORS, DRUG; XENOPUS LAEVIS;

EID: 0037300048     PISSN: 0012186X     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00125-002-1014-3     Document Type: Article

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