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

Sephardic origins revealed for rare skin disorder, recessive dystrophic epidermolysis bullosa, in individuals carrying the unique c.6527insC mutation

携带独特的 c.6527insC 突变的个体患有罕见的皮肤病——隐性营养不良性大疱性表皮松解症,研究发现其起源于塞法迪犹太人。

Warshauer, Emily Mira; Maier, Paul A; Runfeldt, Goran; Fuentes, Ignacia; Escamez, Maria José; Valinotto, Laura; Natale, Monica; Manzur, Graciela; Illera, Nuria; Garcia, Marta; Del Rio, Marcela; Mencia, Angeles; Holguin, Almudena; Larcher, Fernando; Hellenthal, Garrett; Brown, Adam R; Consuegra, Liliana; Rivera, Carolina; Nogueiro, Inês; Tang, Jean; Oro, Anthony; Marinkovich, Peter; Palisson, Francis; Titeux, Matthias; Hovnanian, Alain A; Sprecher, Eli; Skorecki, Karl; Norris, David; Bruckner, Anna; Kogut, Igor; Bilousova, Ganna; Roop, Dennis

A mutation in CCDC50, a gene encoding an effector of epidermal growth factor-mediated cell signaling, causes progressive hearing loss.

CCDC50 基因(编码表皮生长因子介导的细胞信号传导效应因子)发生突变会导致进行性听力丧失

Modamio-Hoybjor Silvia, Mencia Angeles, Goodyear Richard, del Castillo Ignacio, Richardson Guy, Moreno Felipe, Moreno-Pelayo Miguel Angel