Screening of NKX2.5 gene in Moroccan Tetralogy of Fallot patients: worldwide mutation rate compariso...
Screening of NKX2.5 gene in Moroccan Tetralogy of Fallot patients: worldwide mutation rate comparisons show a significant association between R25C variant and TOF phenotype
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Cairo: Springer
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English
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Cairo: Springer
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Background Tetralogy of Fallot is the most prevalent cyanotic congenital heart disease, occurring in 1/3 600 live births. This disorder comprises ventricular septal defect, right ventricular outflow obstruction, over-riding aorta, and right ventricular hypertrophy. The present study aims to reveal the spectrum of Nk2 homeobox 5 (NKX2-5) variants id...
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Full title
Screening of NKX2.5 gene in Moroccan Tetralogy of Fallot patients: worldwide mutation rate comparisons show a significant association between R25C variant and TOF phenotype
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TN_cdi_proquest_journals_2670521801
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https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_journals_2670521801
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ISSN
1110-8630
E-ISSN
2090-2441
DOI
10.1186/s43042-021-00136-1
