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EIF4H

Official Full Name
eukaryotic translation initiation factor 4H
Organism
Homo sapiens
GeneID
7458
Background
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]
Synonyms
WSCR1; WBSCR1; eIF-4H;

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