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Yazeid Alhaidan
Yazeid Alhaidan
Odense University Hospital
Endocrinology
Internal medicine
Exome sequencing
Medicine
Missense mutation
2
Papers
3
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0
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PHKA2 variants expand the phenotype of phosphorylase B kinase deficiency to include patients with ketotic hypoglycemia only
2021
American Journal of Medical Genetics Part A
Anne Benner
Yazeid Alhaidan
Matthew A. Lines
Klaus Brusgaard
Diva D. De León
Rebecca Sparkes
Anja Lisbeth Frederiksen
Henrik Thybo Christesen
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A novel gene in early childhood diabetes: EDEM2 silencing decreases SLC2A2 and PXD1 expression, leading to impaired insulin secretion.
2020
Molecular Genetics and Genomics
Yazeid Alhaidan
Henrik Thybo Christesen
Kurt Højlund
Mohammed Al Balwi
Klaus Brusgaard
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Citations (2)
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