Three cases of Wolfram syndrome with different clinical aspects.

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Authors
Çamtosun, E.
Şıklar, Z.
Kocaay, P.
Ceylaner, S.
Flanagan, Sarah
Ellard, Sian
Berberoğlu, M.
Issue Date
2015-03
Type
Journal Article
Case Report
Language
en
Keywords
Wessex Classification Subject Headings::Oncology. Pathology.::Genetics , Wessex Classification Subject Headings::Endocrinology
Research Projects
Organizational Units
Journal Issue
Alternative Title
Wolfram syndrome is an autosomal recessive disorder caused by mutations in the WFS1 gene. Clinical heterogeneity has been reported both within and between families with WFS1 mutations.
Description
Citation
Three cases of Wolfram syndrome with different clinical aspects. 2015, 28 (3-4):433-8 J. Pediatr. Endocrinol. Metab.
Publisher
De Gruyter
License
Archived with thanks to Journal of pediatric endocrinology & metabolism : JPEM
Journal
Journal of pediatric endocrinology & metabolism : JPEM
Volume
Issue
PubMed ID
ISSN
2191-0251
EISSN