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Functional significance of novel variants of the MEF2C gene promoter in congenital ventricular septal defects

Zeng, ZH; Chen, HX; Liu, XC; Yang, Q; He, GW

He, GW (通讯作者),Tianjin Univ, TEDA Int Cardiovasc Hosp, Tianjin, Peoples R China.

AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2022; 188 (8): 2397

Abstract

Ventricular septal defect (VSD) is the most common congenital heart disease. Although the coding region of MEF2C is highly relevant to cardiac malform......

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