A p.(Glu809Lys) Mutation in the WFS1 Gene Associated with Wolfram-like Syndrome: A Case Report. [electronic resource]
- Journal of clinical research in pediatric endocrinology 12 2016
- 482-483 p. digital
Publication Type: Case Reports; Journal Article
1308-5735
10.4274/jcrpe.3021 doi
Child, Preschool DNA Mutational Analysis Genetic Predisposition to Disease--genetics Humans Male Membrane Proteins--genetics Mutation, Missense Wolfram Syndrome--diagnosis