Generation of two human iPSC lines from patients with maturity-onset diabetes of the young type 2 (MODY2) and permanent neonatal diabetes due to mutations in the GCK gene

Author:

Aqel Yasmin W. Abu,Ali Gowher,Elsayed Ahmed K.,Al-Khawaga Sara,Hussain Khalid,Abdelalim Essam M.

Funder

Qatar Biomedical Research Institute

Publisher

Elsevier BV

Subject

Cell Biology,Developmental Biology,General Medicine

Reference5 articles.

1. Glucokinase (GCK) mutations in hyper- and hypoglycemia: maturity-onset diabetes of the young, permanent neonatal diabetes, and hyperinsulinemia of infancy;Gloyn;Hum. Mutat.,2003

2. Close linkage of glucokinase locus on chromosome 7p to early-onset non-insulin-dependent diabetes mellitus;Froguel;Nature,1992

3. Neonatal diabetes mellitus due to complete glucokinase deficiency;Njolstad;N. Engl. J. Med.,2001

4. The clinical and genetic characteristics of permanent neonatal diabetes (PNDM) in the state of Qatar;Al‐Khawaga;Mol. Genet. Genomic Med.,2019

5. International Standing Committee on Human Cytogenetic Nomenclature., L.G. Shaffer, J. McGowan-Jordan, M. Schmid, ISCN 2013 : an international system for human cytogenetic nomenclature (2013), Karger, Basel, 2013.

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