Do second generation sequencing techniques identify documented genetic markers for neonatal diabetes mellitus?

Author:

Ali Khan ImranORCID

Publisher

Elsevier BV

Subject

Multidisciplinary

Reference154 articles.

1. A homozygous Ier3ip1 mutation causes microcephaly with simplified gyral pattern, epilepsy, and permanent neonatal diabetes syndrome (meds);Abdel-Salam;Am. J. Med. Genet.,2012

2. Neonatal diabetes mellitus;Aguilar-Bryan;Endocr. Rev.,2008

3. Biallelic loss of function variant in the unfolded protein response gene Pdia6 is associated with asphyxiating thoracic dystrophy and neonatal-onset diabetes;Al-Fadhli;Clin. Genet.,2021

4. The clinical and genetic characteristics of permanent neonatal diabetes (pndm) in the state of Qatar;Al-Khawaga;Mol. Gen. Genom. Med.,2019

5. Genetic mutations associated with neonatal diabetes mellitus in Omani patients;Al Senani;J. Pediatr. Endocrinol. Metab.,2018

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