日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Exome sequencing for diagnosis of congenital hemolytic anemia

外显子组测序用于诊断先天性溶血性贫血

Mansour-Hendili, Lamisse; Aissat, Abdelrazak; Badaoui, Bouchra; Sakka, Mehdi; Gameiro, Christine; Ortonne, Valérie; Wagner-Ballon, Orianne; Pissard, Serge; Picard, Véronique; Ghazal, Khaldoun; Bahuau, Michel; Guitton, Corinne; Mansour, Ziad; Duplan, Mylène; Petit, Arnaud; Costedoat-Chalumeau, Nathalie; Michel, Marc; Bartolucci, Pablo; Moutereau, Stéphane; Funalot, Benoît; Galactéros, Frédéric

Alternative splicing at a NAGNAG acceptor site as a novel phenotype modifier.

NAGNAG 受体位点的选择性剪接作为新型表型修饰剂

Hinzpeter Alexandre, Aissat Abdel, Sondo Elvira, Costa Catherine, Arous Nicole, Gameiro Christine, Martin Natacha, Tarze Agathe, Weiss Laurence, de Becdelièvre Alix, Costes Bruno, Goossens Michel, Galietta Luis J, Girodon Emmanuelle, Fanen Pascale