Editorial: Inherited and acquired ribosomopathies: missing puzzle pieces

被引：1

作者：

Valli, Roberto ^{[1
,2
]}

Penzo, Marianna ^{[3
,4
]}

机构：

[1] Univ Insubria, Dept Med & Surg, Varese, Italy

[2] Univ Insubria, Genom Med Ctr, Varese, Italy

[3] Alma Mater Studiorum Univ Bologna, Dept Med & Surg Sci, Bologna, Italy

[4] Alma Mater Studiorum Univ Bologna, Ctr Appl Biomed Res CRBA, Bologna, Italy

来源：

FRONTIERS IN GENETICS | 2023年 / 14卷

关键词：

ribosome biogenesis; rare disease; ribosomopathy; RPL10; shwachman diamond syndrome; diamond blackfan anaemia; X-linked dyskeratosis congenita; T-ALL leukemia; MOLECULAR-BASIS;

D O I：

10.3389/fgene.2023.1194788

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页数：3

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