Publication: Autosomal recessive agammaglobulinemic patient with a novel large deletion in IGHM presenting with mild clinical phenotype
dc.contributor.author | ÖZEN, AHMET OĞUZHAN | |
dc.contributor.authors | Nain, Ercan; Ulgen, Ozge; Kiykim, Ayca; Aydiner, Elif Karakoc; Ozen, Ahmet; Baris, Safa | |
dc.date.accessioned | 2022-03-15T11:46:42Z | |
dc.date.available | 2022-03-15T11:46:42Z | |
dc.date.issued | 2020 | |
dc.identifier.doi | 10.1016/j.clim.2019.108295 | |
dc.identifier.issn | 1521-7035 | |
dc.identifier.pubmed | PMID: 31683053 | |
dc.identifier.uri | https://hdl.handle.net/11424/251696 | |
dc.language.iso | eng | |
dc.relation.ispartof | Clinical Immunology (Orlando, Fla.) | |
dc.rights | info:eu-repo/semantics/closedAccess | |
dc.subject | Humans | |
dc.subject | Male | |
dc.subject | Child, Preschool | |
dc.subject | Phenotype | |
dc.subject | Genes, Recessive | |
dc.subject | Consanguinity | |
dc.subject | Agammaglobulinemia | |
dc.subject | Chromosome Disorders | |
dc.subject | Sequence Deletion | |
dc.subject | Autosomal recessive | |
dc.subject | Clinical variability | |
dc.subject | Heavy Chain Disease | |
dc.subject | IGHM | |
dc.subject | Immunoglobulin mu-Chains | |
dc.title | Autosomal recessive agammaglobulinemic patient with a novel large deletion in IGHM presenting with mild clinical phenotype | |
dc.type | article | |
dspace.entity.type | Publication | |
local.avesis.id | cfdfb60c-cf87-4c9b-9564-3ab7d6549100 | |
local.import.package | SS23 | |
local.import.source | PubMed | |
local.indexed.at | WOS | |
local.indexed.at | SCOPUS | |
local.indexed.at | PUBMED | |
oaire.citation.startPage | 108295 | |
oaire.citation.title | Clinical Immunology (Orlando, Fla.) | |
relation.isAuthorOfPublication | 3e9c297b-e636-4836-8f61-dc9c8b7c29cf | |
relation.isAuthorOfPublication.latestForDiscovery | 3e9c297b-e636-4836-8f61-dc9c8b7c29cf |