KCNQ1 (KvLQT1) missense mutation causing congenital long QT syndrome (Jervell-Lange-Nielsen) in a Mexican family;Detección de una mutación en el gen KCNQ1 (KvLQT1) causante de síndrome de Jervell, Lange-Nielsen en una familia mexicana

Archivos de Cardiologia de Mexico

Volumn 76, Issue 3, 2006, Pages 257-262

  Márquez, Manlio F ^a   Ramos Kuri, Manuel ^b   Hernández Pacheco, Guadalupe ^a   Estrada, Javier ^b   Fabregat, Juan R ^b   Pérez Vielma, Nadia ^a   Gómez Flores, Jorge ^a   González Hermosillo, Antonio ^a   Cárdenas, Manuel ^a   Vargas Alarcón, Gilberto ^a  

^a INSTITUTO NACIONAL DE CARDIOLOGÍA IGNACIO CHÁVEZ   (Mexico)

^b UNIVERSIDAD PANAMERICANA   (Mexico)

Author keywords

Genes; Ionic channels; Long QT syndromes; Mutations

Indexed keywords

POTASSIUM CHANNEL KCNQ1;

ARTICLE; CONGENITAL DISORDER; CONTROLLED STUDY; GENE SEQUENCE; HEARING IMPAIRMENT; HETEROZYGOTE; HUMAN; LONG QT SYNDROME; MEXICO; MISSENSE MUTATION; QT PROLONGATION; SEQUENCE ANALYSIS;

ADOLESCENT; CHILD; CHILD, PRESCHOOL; FEMALE; HUMANS; JERVELL-LANGE NIELSEN SYNDROME; KCNQ1 POTASSIUM CHANNEL; MALE; MEXICO; MUTATION, MISSENSE; PEDIGREE;

EID: 33749606021     PISSN: 14059940     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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