Molecular basis of the clinical features of Holt–Oram syndrome resulting from missense and extended protein mutations of the TBX5 gene as well as TBX5 intragenic duplications
Al-Qattan, Mohammad M., Abou Al-Shaar, HussamVolume:
560
Language:
english
Journal:
Gene
DOI:
10.1016/j.gene.2015.02.017
Date:
April, 2015
File:
PDF, 602 KB
english, 2015