A Novel RAG1 Mutation in a Compound Heterozygous Status in a Child With Omenn Syndrome

RT @FrontGenetics: New Research: A Novel RAG1 Mutation in a Compound Heterozygous Status in a Child With Omenn Syndrome: Omenn syndrome is…

New Research: A Novel RAG1 Mutation in a Compound Heterozygous Status in a Child With Omenn Syndrome: Omenn syndrome is a rare autosomal recessive disorder characterized by severe, combined immunodeficiency and autoimmune features. In this case… https://t.