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

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作者： Dora Janeth,Fonseca ^[1] ; Adrien,Morel ^[1] ; Kevin,Llinás-Caballero ^[1] ; David,Bolívar-Salazar ^[1] ; Paul,Laissue ^[1]

作者单位： Center for Research in Genetics and Genomics-CIGGUR, GENIUROS Research Group, School of Medicine and Health Sciences, Universidad Del Rosario, Bogotá, Colombia. ^[1] BIOPAS Laboratoires, Orphan Diseases Unit, BIOPAS GROUP, Bogotá, Colombia. ^[2]

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

DOI 10.2147/PGPM.S289869

PMID 33688237

发布时间 2022-04-21

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Pharmacogenomics and personalized medicine

2021年14卷

287-299页

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

Pharmacogenomics and personalized medicine

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Pharmacogenomics and personalized medicine

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

Pharmacogenomics and personalized medicine

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Pharmacogenomics and personalized medicine

相关期刊

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