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1دورية أكاديميةAicardi–Goutières syndrome with SAMHD1 deficiency can be diagnosed by unscheduled DNA synthesis test
المؤلفون: Chikako Senju, Yuka Nakazawa, Mayuko Shimada, Dai Iwata, Michiko Matsuse, Katsumi Tanaka, Yasushi Miyazaki, Shinichi Moriwaki, Norisato Mitsutake, Tomoo Ogi
المصدر: Frontiers in Pediatrics, Vol 10 (2022)
مصطلحات موضوعية: Aicardi-Goutières syndrome (AGS), SAMHD1, unscheduled DNA synthesis (UDS), cockayne syndrome (CS), transcription coupled repair (TCR), Pediatrics, RJ1-570
وصف الملف: electronic resource
العلاقة: https://www.frontiersin.org/articles/10.3389/fped.2022.1048002/fullTest; https://doaj.org/toc/2296-2360Test
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المصدر: Frontiers in Pediatrics. 10:1048002
مصطلحات موضوعية: cockayne syndrome (CS), Aicardi-Goutières syndrome (AGS), transcription coupled repair (TCR), SAMHD1, unscheduled DNA synthesis (UDS)
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=jairo_______::f4cd281bf0454fdaaf6733cda7365874Test
http://hdl.handle.net/10069/00042335Test