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1 Ergebnisse
1
Detección de una mutación en el gen KCNQ1 (KvLQT1) causante..:
Márquez, Manlio F
;
Ramos-Kuri, Manuel
;
Hernández-Pacheco, Guadalupe
...
Archivos de cardiología de México v.76 n.3 2006. , 2006
Link:
http://www.scielo.org.mx/scielo.php?script=sci_arttext..
RT Journal T1
Detección de una mutación en el gen KCNQ1 (KvLQT1) causante de síndrome de Jervell, Lange-Nielsen en una familia mexicana
UL https://suche.suub.uni-bremen.de/peid=base-ftscielomexico:oai:scielo:S1405-99402006000300002&Exemplar=1&LAN=DE A1 Márquez, Manlio F A1 Ramos-Kuri, Manuel A1 Hernández-Pacheco, Guadalupe A1 Estrada, Javier A1 RFabregat, Juan A1 Pérez-Vielma, Nadia A1 Gómez-Flores, Jorge A1 González-Hermosillo, Antonio A1 Cárdenas, Manuel A1 Vargas-Alarcón, Gilberto PB Instituto Nacional de Cardiología Ignacio Chávez YR 2006 K1 Canales iónicos K1 Genes K1 Mutaciones K1 Síndrome de QT largo JF Archivos de cardiología de México v.76 n.3 2006 LK http://www.scielo.org.mx/scielo.php?script=sci_arttext&pid=S1405-99402006000300002 DO http://www.scielo.org.mx/scielo.php?script=sci_arttext&pid=S1405-99402006000300002 SF ELIB - SuUB Bremen
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