Nashat Al Sukaiti

Loss of DIAPH1 causes SCBMS, combined immunodeficiency, and mitochondrial dysfunction

Meri Kaustio, Naemeh Nayebzadeh, Reetta Hinttala et al. · Journal of Allergy and Clinical Immunology · 2021 · 47 citations · Full text

Biallelic <scp> <i>ZNFX1</i> </scp> variants are associated with a spectrum of immuno‐hematological abnormalities

Salem Alawbathani, Ana Westenberger, Natalia Ordonez‐Herrera et al. · Clinical Genetics · 2021 · 20 citations

Agammaglobulinaemia despite terminal B‐cell differentiation in a patient with a novel <i>LRBA</i> mutation

Nashat Al Sukaiti, Khwater AbdelRahman, Jalila Alshekaili et al. · Clinical & Translational Immunology · 2017 · 19 citations · Full text

A Decade Experience on Severe Combined Immunodeficiency Phenotype in Oman, Bridging to Newborn Screening

Nashat Al Sukaiti, Khwater Ahmed, Jalila Alshekaili et al. · Frontiers in Immunology · 2021 · 18 citations · Full text

Genetic mutations associated with neonatal diabetes mellitus in Omani patients

Aisha Al Senani, Nishath Hamza, Hanan Al Azkawi et al. · Journal of Pediatric Endocrinology and Metabolism · 2018 · 14 citations · Full text