Noonan syndrome patient-specific induced cardiomyocyte model carrying SOS1 gene variant c.1654A>G-Reference-Cited by-同舟云学术

Noonan syndrome patient-specific induced cardiomyocyte model carrying SOS1 gene variant c.1654A>G

Published:2021-03 Issue:1 Volume:400 Page:112508
ISSN:0014-4827
Container-title:Experimental Cell Research
language:en
Short-container-title:Experimental Cell Research

Author:

Gurusamy Narasimman,Rajasingh Sheeja,Sigamani Vinoth,Rajasingh Reshma,Isai Dona Greta,Czirok Andras^ORCID,Bittel Douglas^ORCID,Rajasingh Johnson^ORCID

Funder

American Heart Association Inc

National Heart Lung and Blood Institute

Publisher

Elsevier BV

Subject

Cell Biology

Reference31 articles.

1. Hypertelorism with Turner phenotype. A new syndrome with associated congenital heart disease;Noonan;Am. J. Dis. Child.,1968

2. Noonan syndrome: a review;Mendez;Am. J. Med. Genet.,1985

3. Noonan syndrome-causing genes: molecular update and an assessment of the mutation rate;El Bouchikhi;Int J Pediatr Adolesc Med,2016

4. Noonan syndrome: clinical aspects and molecular pathogenesis;Tartaglia;Mol Syndromol,2010

5. Germline gain-of-function mutations in SOS1 cause Noonan syndrome;Roberts;Nat. Genet.,2007

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