Cheick O. Guinto
CHU Du Point
Bamako, BKO, Mali
Bamako, BKO, Mali
Last Updated: 09/26/2026
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Found 46 publications
Trio exome analysis is a valuable tool for genetic diagnosis of epilepsy in Mali.
Journal: Genetics in medicine open
Published: January 21, 2025
Using the Fluorescence In Situ Hybridization in the Diagnosis of Trisomy 13 in a Male Newborn From Mali.
Journal: Clinical case reports
Published: December 30, 2024
Rare Variants Cause Charcot-Marie-Tooth Disease in Malian Families.
Journal: Brain and behavior
Published: September 19, 2024
Whole-exome sequencing reveals known and candidate genes for hearing impairment in Mali.
Journal: HGG advances
Published: August 09, 2024
A Novel Splice Site Variant in COL6A1 Causes Ullrich Congenital Muscular Dystrophy in a Consanguineous Malian Family.
Journal: Molecular genetics & genomic medicine
Published: August 05, 2024
Genetic profile of progressive myoclonic epilepsy in Mali reveals novel findings.
Journal: Frontiers in neurology
Published: June 26, 2024
A novel variant in the GNE gene in a Malian patient presenting with distal myopathy.
Journal: Neurogenetics
Published: April 06, 2024
A novel variant in the GNE gene in a Malian patient presenting with distal myopathy.
Journal: Research square
Published: March 18, 2024
AP2A2 mutation and defective endocytosis in a Malian family with hereditary spastic paraplegia.
Journal: Neurobiology of disease
Published: January 13, 2024
Pentanucleotide Repeat Insertions in RAI1 Cause Benign Adult Familial Myoclonic Epilepsy Type 8.
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: July 11, 2023
Socio-cultural representation of epilepsy at the teaching hospital of point G, Mali.
Journal: eNeurologicalSci
Published: July 06, 2023
Last Updated: 09/26/2026