Nain, Ercan <br/><br/>
Autosomal recessive agammaglobulinemic patient with a novel large deletion in IGHM presenting with mild clinical phenotype.  [electronic resource] 

 -  Clinical immunology (Orlando, Fla.)  01 2020 
 - 108295 p.  digital 
<br/><br/> Publication Type: Case Reports; Letter 
<br/><br/><label>ISSN: </label>1521-7035 
<br/><br/><label>Standard No.: </label>10.1016/j.clim.2019.108295  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Agammaglobulinemia--diagnosis<br/>Child, Preschool<br/>Chromosome Disorders<br/>Consanguinity<br/>Genes, Recessive<br/>Heavy Chain Disease--genetics<br/>Humans<br/>Immunoglobulin mu-Chains--genetics<br/>Male<br/>Phenotype<br/>Sequence Deletion--genetics