Recurrent Mutations of the Active Adenylation Domain of UBA1 in Atypical Form of VEXAS Syndrome

Detalles Bibliográficos
Autores principales: Faurel, Alyx, Heiblig, Maël, Kosmider, Olivier, Cornillon, Jérôme, Boudou, Laurence, Guyotat, Denis, Martignoles, Jean-Alain, Jamilloux, Yvan, Noyel, Pauline, Daguenet, Elisabeth, Faure, Anne-Camille, Sujobert, Pierre, Flandrin-Gresta, Pascale
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2023
Materias:
Letter
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10043588/
https://www.ncbi.nlm.nih.gov/pubmed/36999004
http://dx.doi.org/10.1097/HS9.0000000000000868

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10043588/
https://www.ncbi.nlm.nih.gov/pubmed/36999004
http://dx.doi.org/10.1097/HS9.0000000000000868

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