Mek Inhibitor Reverses Hypertrophic Cardiomyopathy in RIT1 Mutated Noonan Syndrome: For the first time, hypertrophic cardiomyopathy was reversed in Noonan syndrome associated with a RIT1 mutation-Reference-Cited by-同舟云学术

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Mek Inhibitor Reverses Hypertrophic Cardiomyopathy in RIT1 Mutated Noonan Syndrome: For the first time, hypertrophic cardiomyopathy was reversed in Noonan syndrome associated with a RIT1 mutation

Published:2019-07-12 Issue:8 Volume:179 Page:1408-1409
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am J Med Genet

Author:

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.40456/fullpdf

Reference3 articles.

1. Hypertrophic cardiomyopathy in Noonan syndrome treated by MEK-inhibition;Andelfinger;J Am Coll Cardiol,2019

2. Cardiomyopathies in Noonan syndrome and the other RASopathies;Gelb;Prog Pediatr Cardiol,2015

3. Emerging RAS superfamily conditions involving GTPase function;Shieh;PLoS Genet,2019

Cited by 4 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. Skeletal defects and bone metabolism in Noonan, Costello and cardio-facio-cutaneous syndromes;Frontiers in Endocrinology;2023-10-27

2. Molecular and clinical profile of patients referred as Noonan or Noonan-like syndrome in Greece: a cohort of 86 patients;European Journal of Pediatrics;2022-07-29

3. Cardiovascular Abnormalities and Gene Mutations in Children With Noonan Syndrome;Frontiers in Genetics;2022-06-13

4. The seventh international RASopathies symposium: Pathways to a cure—expanding knowledge, enhancing research, and therapeutic discovery;American Journal of Medical Genetics Part A;2022-03-09

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