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GATA4 sequence variants in patients with congenital heart disease

BACKGROUND: Recent reports have identified mutations in the transcription factor GATA4 in familial cases of cardiac septal defects. The prevalence of GATA4 mutations in the population of patients with septal defects is unknown. Given that patients with septal and conotruncal defect can share a commo...

詳細記述

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書誌詳細
主要な著者: Tomita‐Mitchell, A, Maslen, C L, Morris, C D, Garg, V, Goldmuntz, E
フォーマット: Artigo
言語:Inglês
出版事項: BMJ Group 2007
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC2652815/
https://ncbi.nlm.nih.gov/pubmed/18055909
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmg.2007.052183
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