EIF2AK3 novel mutation in a child with early-onset diabetes mellitus, a case report

Abstract Background Wolcott-Rallison syndrome (WRS) is caused by a biallelic mutation in the gene encoding eukaryotic translation initiation factor 2-alpha kinase 3 (EIF2AK3) on chromosome 2p11.2. This condition is characterized by permanent early-onset diabetes mellitus, epiphyseal dysplasia, and h...

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Kaituhi matua: Tarah H. Fatani (Author)
Hōputu: Pukapuka
I whakaputaina: BMC, 2019-03-01T00:00:00Z.
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