TY  - GEN
AU  - Şener,Leyla Türker
AU  - Aktan,Melih
AU  - Albeniz,Gürcan
AU  - Şener,Aziz
AU  - Üstek,Duran
AU  - Albeniz,Işıl
TI  - Identification of red blood cell membrane defects in a patient with hereditary spherocytosis using next‑generation sequencing technology and matrix‑assisted laser desorption/ionization time‑of‑flight mass spectrometry
SN  - 1791-3004
PY  - 2019///0819
KW  - Adult
KW  - Aged
KW  - Biomarkers
KW  - analysis
KW  - Case-Control Studies
KW  - Child
KW  - Erythrocyte Membrane
KW  - genetics
KW  - Female
KW  - High-Throughput Nucleotide Sequencing
KW  - methods
KW  - Humans
KW  - Male
KW  - Membrane Proteins
KW  - Middle Aged
KW  - Mutation
KW  - Pedigree
KW  - Phenotype
KW  - Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization
KW  - Spherocytosis, Hereditary
N1  - Publication Type: Case Reports; Journal Article
UR  - https://doi.org/10.3892/mmr.2019.10036
ER  -