Publication:
Autosomal recessive agammaglobulinemic patient with a novel large deletion in IGHM presenting with mild clinical phenotype

Date

Authors

ÖZEN, AHMET OĞUZHAN

Keywords

Humans, Male, Child, Preschool, Phenotype, Genes, Recessive, Consanguinity, Agammaglobulinemia, Chromosome Disorders, Sequence Deletion, Autosomal recessive, Clinical variability, Heavy Chain Disease, IGHM, Immunoglobulin mu-Chains

URI

https://hdl.handle.net/11424/251696

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