Gene symbol: KCNH2.

Human genetics

Volumn 120, Issue 6, 2007, Pages 912-

  Crotti, L ^a   Pedrazzini, M ^a   Ferrandi, C ^a   Insolia, R ^a   Tosin, L ^a   Vicentini, A ^a   Turco, A ^a   De Ferrari, G M ^a   Schwartz, P J ^a  

^a UNIVERSITY OF PAVIA   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

KCNH2 PROTEIN, HUMAN; POTASSIUM CHANNEL HERG; UNCLASSIFIED DRUG; KCNQ1 PROTEIN, HUMAN; POTASSIUM CHANNEL KCNQ1;

ADOLESCENT; AMINO ACID SUBSTITUTION; ARTICLE; CASE REPORT; GENETICS; GILLES DE LA TOURETTE SYNDROME; HUMAN; LONG QT SYNDROME; MALE; MISSENSE MUTATION; CASE CONTROL STUDY; CHILD; FEMALE;

ADOLESCENT; AMINO ACID SUBSTITUTION; ETHER-A-GO-GO POTASSIUM CHANNELS; HUMANS; LONG QT SYNDROME; MALE; MUTATION, MISSENSE; TOURETTE SYNDROME; CASE-CONTROL STUDIES; CHILD; FEMALE; KCNQ1 POTASSIUM CHANNEL;

EID: 34247877734     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (0)