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-Reference-Cited by-同舟云学术

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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

Published:2019-03-14 Issue: Volume: Page:
ISSN:1791-2997
Container-title:Molecular Medicine Reports
language:
Short-container-title:Mol Med Report

Author:

Şener Leyla¹,Aktan Melih²,Albeniz G�rcan³,Şener Aziz⁴,�stek Duran⁵,Albeniz Işıl¹

Affiliation:

1. Department of Biophysics, Istanbul Faculty of Medicine, Istanbul University, 34093 Istanbul, Turkey

2. Department of Hematology, Istanbul Faculty of Medicine, Istanbul University, 34093 Istanbul, Turkey

3. Department of General Surgery, Cerrahpaşa Faculty of Medicine, Istanbul University Cerrahpaşa, 34096 Istanbul, Turkey

4. Department of General Surgery, Kanuni Sultan Suleyman Training and Research Hospital, 34303 Istanbul, Turkey

5. Department of Medical Genetics and REMER, Medipol University, 34810 Istanbul, Turkey

Publisher

Spandidos Publications

Subject

Cancer Research,Oncology,Genetics,Molecular Biology,Molecular Medicine,Biochemistry

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Differentially Expressed Erythrocyte Proteins in Neuromyelitis Optica Spectrum Disorders and Their Functional Annotation Using DAVID Bioinformatics Tool;Neurochemical Journal;2022-12

2. Korean clinical practice guidelines for the diagnosis of hereditary hemolytic anemia;Blood Research;2022-05-20

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