학술논문

Bi-allelic missense disease-causing variants in RPL3L associate neonatal dilated cardiomyopathy with muscle-specific ribosome biogenesis
Document Type
Article
Source
In: Human Genetics. (Human Genetics, 1 November 2020, 139(11):1443-1454)
Subject
Language
English
ISSN
14321203
03406717