Academic Journal

SCN5A-L256del and L1621F exhibit loss-of-function properties related to autosomal recessive congenital cardiac disorders presenting as sick sinus syndrome, dilated cardiomyopathy, and sudden cardiac death

التفاصيل البيبلوغرافية
العنوان: SCN5A-L256del and L1621F exhibit loss-of-function properties related to autosomal recessive congenital cardiac disorders presenting as sick sinus syndrome, dilated cardiomyopathy, and sudden cardiac death
المؤلفون: Shi, Jiaying, Pan, Xueqi, Wang, Zhaokun, Yi, Ming, Xie, Shengyu, Zhang, Xinyue, Tao, Dachang, Yang, Yuan, Liu, Yunqiang
المساهمون: National Natural Science Foundation of China
المصدر: Gene ; volume 898, page 148093 ; ISSN 0378-1119
بيانات النشر: Elsevier BV
سنة النشر: 2024
المجموعة: ScienceDirect (Elsevier - Open Access Articles via Crossref)
نوع الوثيقة: article in journal/newspaper
اللغة: English
DOI: 10.1016/j.gene.2023.148093
الاتاحة: http://dx.doi.org/10.1016/j.gene.2023.148093
https://api.elsevier.com/content/article/PII:S0378111923009344?httpAccept=text/xml
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Rights: https://www.elsevier.com/tdm/userlicense/1.0/ ; https://doi.org/10.15223/policy-017 ; https://doi.org/10.15223/policy-037 ; https://doi.org/10.15223/policy-012 ; https://doi.org/10.15223/policy-029 ; https://doi.org/10.15223/policy-004
رقم الانضمام: edsbas.B8496D38
قاعدة البيانات: BASE
الوصف
DOI:10.1016/j.gene.2023.148093