Abdul A. Zada-Peer
Riyadh, Saudi Arabia
Last Updated: 09/26/2026
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Found 16 publications
Cousin Syndrome Due to TBX15 Gene Variants: Three Novel Cases and Review of the Literature.
Journal: Clinical genetics
Published: January 24, 2026
A novel homozygous CA5A gene deletion in carbonic anhydrase VA deficiency presenting as developmental delay without metabolic crisis.
Journal: Molecular genetics and metabolism reports
Published: December 03, 2025
Aggressive Disease and Poor Clinical Outcome in CEBPα-Mutated Acute Myeloid Leukemia Patient.
Journal: Clinical case reports
Published: July 22, 2025
Clinical and molecular characterization of hepatic glycogen storage disease in Saudi Arabia.
Journal: PloS one
Published: March 20, 2025
Novel de novo heterozygous CACNA1A gene variant in generalised dystonia: a case report.
Journal: BMJ neurology open
Published: May 26, 2024
Incidence of Inborn Errors of Metabolism and Endocrine Disorders Among 40965 Newborn Infants at Riyadh Second Health Cluster of the Ministry of Health Saudi Arabia.
Journal: International journal of neonatal screening
Published: April 29, 2024
A rare presentation of BCR-ABL1 and RUNX1-MECOM rearrangement in a pediatric patient with acute myeloid leukemia.
Journal: Clinical case reports
Published: January 31, 2024
Favorable outcome of PML-RARα short isoform and FLT3-ITD mutation in a patient with several adverse prognostic markers: A case report.
Journal: Clinical case reports
Published: April 13, 2023
Fatal intracranial haemorrhage in acute promyelocytic leukemia patients with short isoform of PML-RARα: Review of molecular and radiological data.
Journal: Saudi journal of biological sciences
Published: January 24, 2023
Atypical presentation of adenosine deaminase 2 deficiency with bi-allelic ADA2 mutation.
Journal: Clinical case reports
Published: December 14, 2021
Development of simple and effective PCR based assay to detect PCCA mutation (c.425G > A) among Saudi carriers and functional study of the homozygous PCCA mutations.
Journal: Saudi journal of biological sciences
Published: September 01, 2021
New paradigms of USP53 disease: normal GGT cholestasis, BRIC, cholangiopathy, and responsiveness to rifampicin.
Journal: Journal of human genetics
Published: March 25, 2020
Last Updated: 09/26/2026