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Charras, Amandine ORCID: 0000-0001-6760-5459, Haldenby, Sam, Smith, Eve MD, Egbivwie, Naomi, Olohan, Lisa, Kenny, John G, Schwarz, Klaus, Roberts, Carla, Al-Abadi, Eslam, Armon, Kate et al (show 17 more authors)
(2022)
Panel sequencing links rare, likely damaging gene variants with distinct clinical phenotypes and outcomes in juvenile-onset SLE.
Rheumatology (Oxford, England).
keac275 - ?.