Şener, Leyla Türker <br/><br/>
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.  [electronic resource] 

 -  Molecular medicine reports  May 2019 
 - 3912-3922 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1791-3004 
<br/><br/><label>Standard No.: </label>10.3892/mmr.2019.10036  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Aged<br/>Biomarkers--analysis<br/>Case-Control Studies<br/>Child<br/>Erythrocyte Membrane--genetics<br/>Female<br/>High-Throughput Nucleotide Sequencing--methods<br/>Humans<br/>Male<br/>Membrane Proteins--genetics<br/>Middle Aged<br/>Mutation<br/>Pedigree<br/>Phenotype<br/>Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization--methods<br/>Spherocytosis, Hereditary--genetics