Lettilia Xhakaza
Bellville, WC, South Africa
Last Updated: 09/26/2026
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Found 10 publications
Exome sequencing identifies known and candidate genes in hearing impairment in Cameroon.
Journal: Communications medicine
Published: April 02, 2025
Exome sequencing identifies known and candidate genes in hearing impairment in Cameroon.
Journal: Communications medicine
Published: April 02, 2025
Bi-Allelic MARVELD2 Variant Identified with Exome Sequencing in a Consanguineous Multiplex Ghanaian Family Segregating Non-Syndromic Hearing Loss.
Journal: International journal of molecular sciences
Published: February 28, 2025
Exome sequencing revealed a novel homozygous variant in TRMT61 A in a multiplex family with atypical Cornelia de Lange Syndrome from Rwanda.
Journal: BMC medical genomics
Published: January 28, 2025
The Diverse Genetic Landscape of Hearing Impairment in South African Families.
Journal: Clinical genetics
Published: January 22, 2025
Genetic Association of Solute Carrier Transporter Gene Variants with Metformin Response.
Journal: Balkan journal of medical genetics : BJMG
Published: August 27, 2021
Socio-demographic and modifiable risk factors of diabetes and hypertension among resource constrained patients from rural areas in Mdantsane Township in South Africa.
Journal: African health sciences
Published: January 06, 2021
Evaluation of the suitability of 19 pharmacogenomics biomarkers for individualized metformin therapy for type 2 diabetes patients.
Journal: Drug metabolism and personalized therapy
Published: April 01, 2020
Evaluation of the suitability of 19 pharmacogenomics biomarkers for individualized metformin therapy for type 2 diabetes patients.
Journal: Drug metabolism and personalized therapy
Published: April 01, 2020
Effect of the African-specific promoter polymorphisms on the SLC22A2 gene expression levels.
Journal: Drug metabolism and personalized therapy
Published: November 28, 2017
Showing 1-10 of 10
Last Updated: 09/26/2026