机译:NFATC1 NFATC1中的杂合畸形突变与房室间隔缺损有关
IRCCS NeuromedLocalita` Camerelle86077 Pozzilli Italy;
Hubrecht Institute‐KNAW and University Medical Center Utrecht3584CT Utrecht The Netherlands;
Molecular Genetics Unit Casa Sollievo della Sofferenza HospitalIRCCS71013 San Giovanni Rotondo;
Molecular Genetics Unit Casa Sollievo della Sofferenza HospitalIRCCS71013 San Giovanni Rotondo;
Molecular Genetics Unit Casa Sollievo della Sofferenza HospitalIRCCS71013 San Giovanni Rotondo;
Genetics and Rare Diseases Research DivisionIRCCS00146 Rome Italy;
Division of Pediatric Cardiology“Sapienza” University00161 Rome Italy;
IRCCS NeuromedLocalita` Camerelle86077 Pozzilli Italy;
Genetics and Rare Diseases Research DivisionIRCCS00146 Rome Italy;
Molecular Genetics Unit Casa Sollievo della Sofferenza HospitalIRCCS71013 San Giovanni Rotondo;
Molecular Genetics Unit Casa Sollievo della Sofferenza HospitalIRCCS71013 San Giovanni Rotondo;
Molecular Genetics Unit Casa Sollievo della Sofferenza HospitalIRCCS71013 San Giovanni Rotondo;
Bioinformatics Unit Casa Sollievo della Sofferenza HospitalIRCCS71013 San Giovanni Rotondo Italy;
Genetics and Rare Diseases Research DivisionIRCCS00146 Rome Italy;
Genetics and Rare Diseases Research DivisionIRCCS00146 Rome Italy;
Genetics and Rare Diseases Research DivisionIRCCS00146 Rome Italy;
Division of Pediatric Cardiology“Sapienza” University00161 Rome Italy;
Hubrecht Institute‐KNAW and University Medical Center Utrecht3584CT Utrecht The Netherlands;
Molecular Genetics Unit Casa Sollievo della Sofferenza HospitalIRCCS71013 San Giovanni Rotondo;
Atrioventricular septal defect; congenital heart defect; heterotaxy; NFATC1; oculo‐auriculo‐vertebral spectrum;
机译:NFATC1 NFATC1中的杂合畸形突变与房室间隔缺损有关
机译:NFATc1基因多态性与中国汉族人群室间隔缺损的关系
机译:NFATc1中的串联重复多态性与中国人群膜周室间隔缺损风险增加相关。
机译:两种畸形突变在人心房颤动中的血液发生影响的仿真研究
机译:非综合征性房室间隔缺损:初次修复后左房室瓣膜置换的精确定义,相关危险因素和预后因素。
机译:CRELD1的错义突变与心脏房室间隔缺损相关。
机译:异常综合征的畸形突变特异性突变协会inceld1with心脏病内平静缺陷