Clinical analysis of Noonan syndrome caused by RRAS2 mutations and literature review
Author:
Publisher
Elsevier BV
Subject
Genetics (clinical),Genetics,General Medicine
Reference19 articles.
1. R-ras gtpases signaling role in myelin neurodegenerative diseases;Alcover-Sanchez;Int. J. Mol. Sci.,2020
2. Cutaneous t-cell lymphoma in shoc2 mutation-associated noonan-like syndrome with loose anagen hair;Avery;JAAD case reports,2022
3. Activating mutations of rras2 are a rare cause of noonan syndrome;Capri;Am. J. Hum. Genet.,2019
4. Characterization of four novel ras-like genes expressed in a human teratocarcinoma cell line;Drivas;Mol. Cell Biol.,1990
5. R-ras1 and r-ras2 expression in anatomical regions and cell types of the central nervous system;Garcia-Martin;Int. J. Mol. Sci.,2022
Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Functional analysis of RRAS2 pathogenic variants with a Noonan-like phenotype;Frontiers in Genetics;2024-03-27
2. The RRAS2 pathogenic variant (c.67G>T; p. Gly23Cys) produces Noonan syndrome with embryonal rhabdomyosarcoma;Molecular Genetics & Genomic Medicine;2023-11-09
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