Molecular basis of Kir6.2 mutations associated with neonatal diabetes or neonatal diabetes plus neurological features

Proceedings of the National Academy of Sciences of the United States of America

Volumn 101, Issue 50, 2004, Pages 17539-17544

  Proks, Peter ^a   Antcliff, Jennifer F ^a   Lippiat, Jon ^a   Gloyn, Anna L ^b,c   Hattersley, Andrew T ^b   Ashcroft, Frances M ^a  

^a UNIVERSITY OF OXFORD   (United Kingdom)

^b PENINSULA MEDICAL SCHOOL   (United Kingdom)

^c CHURCHILL HOSPITAL   (United Kingdom)

Author keywords

ATP binding site; KATP channel; KCNJ11; Potassium channel

Indexed keywords

INWARDLY RECTIFYING POTASSIUM CHANNEL SUBUNIT KIR6.2; SULFONYLUREA RECEPTOR;

ARTICLE; CONTROLLED STUDY; DIABETES MELLITUS; DISEASE SEVERITY; GENE EXPRESSION; GENE MUTATION; HUMAN; NEUROLOGIC DISEASE; NEWBORN DISEASE; NONHUMAN; NUCLEOTIDE SEQUENCE; OOCYTE; PHENOTYPE; PRIORITY JOURNAL; RAT; XENOPUS;

ADENOSINE TRIPHOSPHATE; ANIMALS; ATP-BINDING CASSETTE TRANSPORTERS; DIABETES COMPLICATIONS; DIABETES MELLITUS; ELECTROPHYSIOLOGY; HUMANS; INFANT, NEWBORN; ION CHANNEL GATING; KINETICS; MULTIDRUG RESISTANCE-ASSOCIATED PROTEINS; MUTATION; NERVOUS SYSTEM DISEASES; OOCYTES; POTASSIUM CHANNELS, INWARDLY RECTIFYING; RATS; SULFONYLUREA COMPOUNDS; XENOPUS LAEVIS;

EID: 10644233000     PISSN: 00278424     EISSN: None     Source Type: Journal    
DOI: 10.1073/pnas.0404756101     Document Type: Article

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