基因名：
EIF4H
产品别名：
WBSCR1； WSCR1； eIF-4H； EIF4H； eukaryotic translation initiation factor 4H； eukaryotic translation initiation factor 4H； eukaryotic translation initiation factor 4H； Williams-Beuren syndrome chromosome region 1； eIF4H蛋白； 真核翻译起始因子4H(EIF4H)；
背景信息：
This gene encodes one of the translation initiation factors, which functions to stimulate the initiation of protein synthesis at the level of mRNA utilization. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. Alternative splicing of this gene generates 2 transcript variants. [provided by RefSeq, Jul 2008]
