Associated Papers
Whole-Exome Sequencing in Patients Affected by Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis Reveals New Variants Potentially Contributing to the Phenotype.
Fonseca DJ et al.
Pharmacogenomics and Personalized Medicine, 2021
Loss of UGP2 in brain leads to a severe epileptic encephalopathy, emphasizing that bi-allelic isoform-specific start-loss mutations of essential genes can cause genetic diseases.
Perenthaler E et al.
Acta Neuropathologica, 2020
31820119 (PubMed )
Supplement: 401_2019_2109_MOESM10_ESM.xls › 247_Genes_LOF
Mutant GNLY is linked to Stevens-Johnson syndrome and toxic epidermal necrolysis.
Fonseca DJ et al.
Human Genetics, 2019
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