Literature DB >> 29516126

A De Novo Novel Nonsense Mutation of GATA4 is Responsible for a Patient with Atrial Septal Defect.

Lv Liu1, Rong Yu2.   

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Year:  2018        PMID： 29516126     DOI： 10.1007/s00246-018-1835-6

Source DB:  PubMed          Journal:  Pediatr Cardiol        ISSN： 0172-0643            Impact factor:   1.655


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  4 in total

1.  Germline mutations in NKX2-5, GATA4, and CRELD1 are rare in a Mexican sample of Down syndrome patients with endocardial cushion and septal heart defects.

Authors:  Miguel A Alcántara-Ortigoza; Jesús De Rubens-Figueroa; Miriam E Reyna-Fabian; Bernardette Estandía-Ortega; Ariadna González-del Angel; Bertha Molina-Álvarez; José A Velázquez-Aragón; Sandra Villagómez-Martínez; Gabriela I Pereira-López; Víctor Martínez-Cruz; Víctor Cruz-Martínez; Rosa M Álvarez-Gómez; Luisa Díaz-García; Luisa García-Díaz
Journal:  Pediatr Cardiol       Date:  2014-12-19       Impact factor: 1.655

2.  Exome Sequencing Identifies a Novel DES Mutation (R227C) in a Chinese Dilated Cardiomyopathy Family.

Authors:  Rong Yu; Lv Liu; Chan Chen; Jin-Mei Shen
Journal:  Cardiology       Date:  2017-02-08       Impact factor: 1.869

3.  Congenital Heart Disease: The Remarkable Journey From the "Post-Mortem Room" to Adult Clinics.

Authors:  Ali J Marian
Journal:  Circ Res       Date:  2017-03-17       Impact factor: 17.367

Review 4.  Genetics of congenital heart disease: the glass half empty.

Authors:  Akl C Fahed; Bruce D Gelb; J G Seidman; Christine E Seidman
Journal:  Circ Res       Date:  2013-02-15       Impact factor: 17.367
  4 in total

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