Editorial: Whole Genome Sequencing for rare diseases

被引：1
|
作者：
Di Resta, Chiara [1 ,2 ]
D'Argenio, Valeria [3 ,4 ]
机构：
[1] Univ Vita Salute San Raffaele, Fac Med, Milan, Italy
[2] IRCCS San Raffaele Sci Inst, Genom Unit Diag Human Pathol, Milan, Italy
[3] San Raffaele Open Univ, Dept Human Sci & Qual Life Promot, Rome, Italy
[4] CEINGE Biotecnol Avanzate Franco Salvatore, Naples, Italy
来源：
FRONTIERS IN MEDICINE | 2023年 / 10卷
关键词：
rare diseases; Whole Genome Sequencing; diagnosis; treatment; pathogenesis;
D O I：
10.3389/fmed.2023.1267930
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
引用
收藏
页数：3
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