揭开基因（抽搐）疗法的神秘面纱。

IF 1.6 4区医学 Q3 GENETICS & HEREDITY European journal of medical genetics Pub Date : 2024-07-26 DOI:10.1016/j.ejmg.2024.104963

Chun-Hung Chan , David A. Pearce

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引用次数: 0

摘要

本文总结了 2023 年 3 月 14-15 日在德国柏林举行的 RE（ACT）大会和 IRDiRC 联席会议上题为 "揭开基因疗法的神秘面纱 "分会的讨论情况。本次会议的重点是讨论基因疗法不断变化的前景，以及当前是否有资源为研究人员、临床医生、患者权益倡导者、立法者以及患者及其家属等利益相关者提供充分的教育。本文的目的不是全面概述基因疗法的现状，而是重点介绍可能有助于 "揭开 "无数基因疗法神秘面纱的资源。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

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Demystifying gene(tic) therapies

This article summarizes the discussion from a session entitled “Demystifying gene therapies” that was held at the joint RE(ACT) congress and IRDiRC conference, 14–15 March 2023 in Berlin, Germany. The focus of this session was to discuss the changing landscape of genetic therapies and whether current resources exist to provide adequate education to stakeholders, such as researchers, clinicians, patient advocates, legislators, as well as the patients and their families. The goal of this article is not to provide a comprehensive overview of the current landscape in genetic therapies, but rather to highlight resources that may be useful to help “demystify” the myriad of genetic therapeutic approaches.

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来源期刊

European journal of medical genetics 医学-遗传学

CiteScore

4.10

自引率

0.00%

发文量

193

审稿时长

66 days

期刊介绍： The European Journal of Medical Genetics (EJMG) is a peer-reviewed journal that publishes articles in English on various aspects of human and medical genetics and of the genetics of experimental models. Original clinical and experimental research articles, short clinical reports, review articles and letters to the editor are welcome on topics such as : • Dysmorphology and syndrome delineation • Molecular genetics and molecular cytogenetics of inherited disorders • Clinical applications of genomics and nextgen sequencing technologies • Syndromal cancer genetics • Behavioral genetics • Community genetics • Fetal pathology and prenatal diagnosis • Genetic counseling.