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Search results (9)

« Back to Publications

Direct correction of haemoglobin E β-thalassaemia using base editors.

Badat M. et al, (2023), Nat Commun, 14

Acquired haemophilia A diagnosed during pregnancy.

Ejaz A. et al, (2023), Obstet Med, 16, 56 - 58

A unified model of human hemoglobin switching through single-cell genome editing.

Shen Y. et al, (2021), Nat Commun, 12

Uridine-responsive epileptic encephalopathy due to inherited variants in CAD: A Tale of Two Siblings.

McGraw CM. et al, (2021), Ann Clin Transl Neurol, 8, 716 - 722

Long-Term Patient-Customized Therapy for a Pathogenic EPO Mutation.

Ejaz A. et al, (2021), Med, 2, 33 - 37.e1

Diagnosis and management of primary immune thrombocytopenia in adults.

Ejaz A. and Radia D., (2019), Br J Hosp Med (Lond), 80, C54 - C57

Somatic copy number gains of α-synuclein (SNCA) in Parkinson's disease and multiple system atrophy brains.

Mokretar K. et al, (2018), Brain, 141, 2419 - 2431

Regulation of Corticosteroidogenic Genes by MicroRNAs.

Robertson S. et al, (2017), Int J Endocrinol, 2017

DNA isolation protocol effects on nuclear DNA analysis by microarrays, droplet digital PCR, and whole genome sequencing, and on mitochondrial DNA copy number estimation.

Nacheva E. et al, (2017), PLoS One, 12