Cargando…
Whole exome sequencing in childhood-onset lupus frequently detects single gene etiologies
BACKGROUND: Systemic lupus erythematosus (SLE) comprise a diverse range of clinical manifestations. To date, more than 30 single gene causes of lupus/lupus like syndromes in humans have been identified. In the clinical setting, identifying the underlying molecular diagnosis is challenging due to phe...
Autores principales: | Tirosh, Irit, Spielman, Shiri, Barel, Ortal, Ram, Reut, Stauber, Tali, Paret, Gideon, Rubinsthein, Marina, Pessach, Itai M., Gerstein, Maya, Anikster, Yair, Shukrun, Rachel, Dagan, Adi, Adler, Katerina, Pode-Shakked, Ben, Volkov, Alexander, Perelman, Marina, Greenberger, Shoshana, Somech, Raz, Lahav, Einat, Majmundar, Amar J., Padeh, Shai, Hildebrandt, Friedhelm, Vivante, Asaf |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6668194/ https://www.ncbi.nlm.nih.gov/pubmed/31362757 http://dx.doi.org/10.1186/s12969-019-0349-y |
Ejemplares similares
-
Progressive Pseudorheumatoid Dysplasia resolved by whole exome sequencing: a novel mutation in WISP3 and review of the literature
por: Pode-Shakked, Ben, et al.
Publicado: (2019) -
Cardiac failure in very long chain acyl-CoA dehydrogenase deficiency requiring extracorporeal membrane oxygenation (ECMO) treatment: A case report and review of the literature
por: Katz, Sharon, et al.
Publicado: (2016) -
Glutaric Aciduria type I and acute renal failure — Coincidence or causality?
por: Pode-Shakked, Ben, et al.
Publicado: (2014) -
Effect of interleukin-1 antagonist on growth of children with colchicine resistant or intolerant FMF
por: Pinchevski-Kadir, Shiran, et al.
Publicado: (2023) -
Hereditary neuropathy with liability to pressure palsies (HNPP): Intrafamilial phenotypic variability and early childhood refusal to walk as the presenting symptom
por: Karklinsky, Shani, et al.
Publicado: (2022)