Expanding the Clinical Spectrum Associated With GLIS3 Mutations.

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Authors
Dimitri, P.
Habeb, A. M.
Gurbuz, F.
Millward, A.
Wallis, S.
Moussa, K.
Akcay, T.
Taha, D.
Hogue, J.
Slavotinek, A.
Issue Date
2015-10
Type
Journal Article
Research Support, Non-U.S. Gov't
Language
en
Keywords
Wessex Classification Subject Headings::Oncology. Pathology.::Genetics , Wessex Classification Subject Headings::Endocrinology::Diabetes
Research Projects
Organizational Units
Journal Issue
Alternative Title
GLIS3 (GLI-similar 3) is a member of the GLI-similar zinc finger protein family encoding for a nuclear protein with 5 C2H2-type zinc finger domains. The protein is expressed early in embryogenesis and plays a critical role as both a repressor and activator of transcription. Human GLIS3 mutations are extremely rare.
Description
Citation
Expanding the Clinical Spectrum Associated With GLIS3 Mutations. 2015, 100 (10):E1362-9 J. Clin. Endocrinol. Metab.
Publisher
Endocrine Society
License
Archived with thanks to The Journal of clinical endocrinology and metabolism
Journal
The Journal of Clinical Endocrinology and Metabolism
Volume
Issue
PubMed ID
ISSN
1945-7197
EISSN