Whole-Exome Sequencing in Patients Affected by Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis Reveals New Variants Potentially Contributing to the Phenotype.

Fonseca, Dora Janeth; Morel, Adrien; Llinás-Caballero, Kevin; Bolívar-Salazar, David; Laissue, Paul

Fonseca, Dora Janeth; Morel, Adrien; Llinás-Caballero, Kevin; Bolívar-Salazar, David; Laissue, Paul.

Afiliación

Fonseca DJ; Center for Research in Genetics and Genomics-CIGGUR, GENIUROS Research Group, School of Medicine and Health Sciences, Universidad Del Rosario, Bogotá, Colombia.
Morel A; Center for Research in Genetics and Genomics-CIGGUR, GENIUROS Research Group, School of Medicine and Health Sciences, Universidad Del Rosario, Bogotá, Colombia.
Llinás-Caballero K; Center for Research in Genetics and Genomics-CIGGUR, GENIUROS Research Group, School of Medicine and Health Sciences, Universidad Del Rosario, Bogotá, Colombia.
Bolívar-Salazar D; Center for Research in Genetics and Genomics-CIGGUR, GENIUROS Research Group, School of Medicine and Health Sciences, Universidad Del Rosario, Bogotá, Colombia.
Laissue P; Center for Research in Genetics and Genomics-CIGGUR, GENIUROS Research Group, School of Medicine and Health Sciences, Universidad Del Rosario, Bogotá, Colombia.

Pharmgenomics Pers Med ; 14: 287-299, 2021.

Article en En | MEDLINE | ID: mdl-33688237

Palabras clave

Stevens-Johnson syndrome; molecular aetiology; toxic epidermal necrolysis; whole-exome sequencing

Texto completo

Añadir a Mi BVS

Imprimir

XML

PubMed Links

Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Pharmgenomics Pers Med Año: 2021 Tipo del documento: Article País de afiliación: Colombia Pais de publicación: Nueva Zelanda

Texto completo

Añadir a Mi BVS

Imprimir

XML

PubMed Links

Buscar en Google