Variable loss of Kir4.1 channel function in SeSAME syndrome mutations

Biochemical and Biophysical Research Communications

Volumn 399, Issue 4, 2010, Pages 537-541

  Tang, Xiaofang ^a   Hang, Darwin ^a   Sand, Andrea ^a   Kofuji, Paulo ^a  

^a UNIVERSITY OF MINNESOTA   (United States)

Author keywords

EAST syndrome; Glia; KCNJ10; Kir4.1; SeSAME syndrome

Indexed keywords

POTASSIUM CHANNEL; POTASSIUM CHANNEL KIR4.1; UNCLASSIFIED DRUG; INWARDLY RECTIFYING POTASSIUM CHANNEL; KCNJ10 (CHANNEL);

ARTICLE; ATAXIA; BIOTINYLATION; CELL MEMBRANE; CELL STRAIN HEK293; ELECTROLYTE DISTURBANCE; ELECTROPHYSIOLOGY; LOSS OF FUNCTION MUTATION; MENTAL DEFICIENCY; NONSENSE MUTATION; PERCEPTION DEAFNESS; PRIORITY JOURNAL; PROTEIN EXPRESSION; SEIZURE; SESAME SYNDROME; WILD TYPE; ANIMAL; CELL LINE; GENETICS; HUMAN; INTELLECTUAL IMPAIRMENT; METABOLIC DISORDER; METABOLISM; MUTATION; RAT; SYNDROME;

ANIMALS; ATAXIA; BIOTINYLATION; CELL LINE; HEARING LOSS, SENSORINEURAL; HUMANS; MENTAL RETARDATION; MUTATION; POTASSIUM CHANNELS, INWARDLY RECTIFYING; RATS; SEIZURES; SYNDROME; WATER-ELECTROLYTE IMBALANCE; INTELLECTUAL DISABILITY;

MAMMALIA; SESAMUM INDICUM;

EID: 77956265369     PISSN: 0006291X     EISSN: 10902104     Source Type: Journal    
DOI: 10.1016/j.bbrc.2010.07.105     Document Type: Article

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