Article
A heterozygous mutation in the RAG2 gene with cutaneous and systemic manifestations partially resembling Omenn syndrome.
Journal der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG - 1 Jun 2021
Estébanez Andrea, Verdú-Amorós Jaime, Silva Esmeralda, Velasco Rebeca, Cuesta Ana, Monteagudo Carlos, Martín Jose M
Abstract excerpt
No abstract is available from the source.
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.
