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Whole exome sequencing and rare variant association study to identify genetic modifiers, KLF1 mutations, and a novel double mutation in Thai patients with hemoglobin E/beta-thalassemia
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- المؤلفون: Hantaweepant, Chattree; Suktitipat, Bhoom; Pithukpakorn, Manop; Chinthammitr, Yingyong; Limwongse, Chanin; Tansiri, Nawaporn; Sawatnatee, Surasak; Takpradit, Chayamon; Rotchanapanya, Wannaphorn; Pongudom, Saranya; Charoenprasert, Kanyaporn; Paiboonsukwong, Kittiphong; Thamprasert, Wichuda; Nolwachai, Narumol; Rattanasawat, Wanlapa; Sae-Aeng, Busakorn; Khorwanichakij, Nisachon; Saetow, Putchong; Saengboon, Supawee; Kamjornpreecha, Krittichat; Pholmoo, Wikanda; Dujjawan, Boonyanuch; Siritanaratkul, Noppadol
- المصدر:
Hematology ; volume 28, issue 1 ; ISSN 1607-8454
- نوع التسجيلة:
article in journal/newspaper
- اللغة:
English
- معلومة اضافية
- Contributors:
National Human Genome Research Institute and the National Heart, Lung, and Blood Institute
- بيانات النشر:
Informa UK Limited
- الموضوع:
2023
- الرقم المعرف:
10.1080/16078454.2023.2187155
- Rights:
http://creativecommons.org/licenses/by/4.0/
- الرقم المعرف:
edsbas.5A1C6FA8
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