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Author

Fatima Alabdulrazzaq

ORCID: 0009-0003-0052-8163
Observed ORCID: 0009-0003-0052-8163
OpenAlex ID: A5083461150
Expanding the allelic spectrum of ELOVL4‐related autosomal recessive neuro‐ichthyosis
2023 · Fatima Alabdulrazzaq, Talal Alanzi, et al. · Molecular Genetics & Genomic Medicine · 7
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TTC19-related mitochondrial complex III deficiency: Clinical and genetic characterization of 10 patients from 5 unrelated Arab families
2026 · Malak Alghamdi, Ahmad Alahmad, et al. · Molecular Genetics and Metabolism · 2
eP001: Newborn screening experience for very long chain Acyl-CoA Dehydrogenase (VLCAD) deficiency in Kuwait
2022 · Fatima Alabdulrazzaq, Hind AlSharhan, et al. · Genetics in Medicine · 2
Works count: 3
Citation count: 11
H-index: 2
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