Pediatrics
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28 march 2019 21:02:39 |
| EIF2AK3 novel mutation in a child with early-onset diabetes mellitus, a case report (BMC Pediatrics) |
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Tweet 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 ... |
| 59 viewsCategory: Pediatrics |
 Clinically relevant body composition methods for obese pediatric patients (BMC Pediatrics)Congenital emphysematous lung disease associated with a novel Filamin A mutation. Case report and literature review (BMC Pediatrics) 
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