Faten B. Almutairi
Riyadh, 11211, Saudi Arabia
Last Updated: 09/26/2026
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Found 8 publications
Humoral Immune Response to SARS-CoV-2 in Children with Idiopathic Nephrotic Syndrome: A Cross-Sectional Exploratory Study.
Journal: International journal of general medicine
Published: January 31, 2026
Bi-allelic variants in HOPS complex subunit VPS41 cause cerebellar ataxia and abnormal membrane trafficking.
Journal: Brain : a journal of neurology
Published: April 27, 2020
Genetic and phenotypic characterization of NKX6-2-related spastic ataxia and hypomyelination.
Journal: European journal of neurology
Published: April 24, 2019
A Novel Homozygous Mutation in SPTBN2 Leads to Spinocerebellar Ataxia in a Consanguineous Family: Report of a New Infantile-Onset Case and Brief Review of the Literature.
Journal: Cerebellum (London, England)
Published: December 03, 2017
Identification of novel genomic imbalances in Saudi patients with congenital heart disease.
Journal: Molecular cytogenetics
Published: September 13, 2017
Further delineation of the phenotypic spectrum of ISCA2 defect: A report of ten new cases.
Journal: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society
Published: April 03, 2017
KCNA4 deficiency leads to a syndrome of abnormal striatum, congenital cataract and intellectual disability.
Journal: Journal of medical genetics
Published: November 12, 2015
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Last Updated: 09/26/2026