The p.(Glu809Lys) mutation in the WFS1 gene is associated with the occurrence of the Wolfram-like syndrome-WFSL: a case report.
CONCLUSIONS: The mutation p.(Glu809Lys) in the WFS1 gene is associated with the occurrence of the Wolfram-like syndrome-WFSL.
PMID: 27217304 [PubMed - as supplied by publisher]
Source: JCRPE Journal of Clinical Research in Pediatric Endocrinology - Category: Endocrinology Tags: J Clin Res Pediatr Endocrinol Source Type: research
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