Neonatal Diabetes Mellitus with Congenital Hypothyroidism
Author:
Publisher
Springer International Publishing
Link
https://link.springer.com/content/pdf/10.1007/978-3-319-66816-1_1841-1
Reference8 articles.
1. Alghamdi KA, Alsaedi AB, Aljasser A, Altawil A, Kamal NM (2017) Extended clinical features associated with novel Glis3 mutation: a case report. BMC Endocr Disord 17:14. https://doi.org/10.1186/s12902-017-0160-z
2. Beak JY, Kang HS, Kim YS, Jetten AM (2007) Krüppel-like zinc finger protein Glis3 promotes osteoblast differentiation by regulating FGF18 expression. J Bone Miner Res 22:1234–1244. https://doi.org/10.1359/jbmr.070503
3. Dimitri P et al (2015) Expanding the clinical spectrum associated with GLIS3 mutations. J Clin Endocrinol Metab 100:E1362–E1369. https://doi.org/10.1210/jc.2015-1827
4. Dimitri P et al (2011) Novel GLIS3 mutations demonstrate an extended multisystem phenotype. Eur J Endocrinol 164:437–443. https://doi.org/10.1530/eje-10-0893
5. Kim YS, Nakanishi G, Lewandoski M, Jetten AM (2003) GLIS3, a novel member of the GLIS subfamily of Krüppel-like zinc finger proteins with repressor and activation functions. Nucleic Acids Res 31:5513–5525. https://doi.org/10.1093/nar/gkg776
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