TY  - GEN
AU  - Nain,Ercan
AU  - Ulgen,Ozge
AU  - Kiykim,Ayca
AU  - Aydiner,Elif Karakoc
AU  - Ozen,Ahmet
AU  - Baris,Safa
TI  - Autosomal recessive agammaglobulinemic patient with a novel large deletion in IGHM presenting with mild clinical phenotype
SN  - 1521-7035
PY  - 2020///0731
KW  - Agammaglobulinemia
KW  - diagnosis
KW  - Child, Preschool
KW  - Chromosome Disorders
KW  - Consanguinity
KW  - Genes, Recessive
KW  - Heavy Chain Disease
KW  - genetics
KW  - Humans
KW  - Immunoglobulin mu-Chains
KW  - Male
KW  - Phenotype
KW  - Sequence Deletion
N1  - Publication Type: Case Reports; Letter
UR  - https://doi.org/10.1016/j.clim.2019.108295
ER  -