Thanh V. Ta
1st Ton That Tung Street, Hanoi 11521
Hanoi, Viet Nam
Hanoi, Viet Nam
Last Updated: 09/26/2026
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Found 16 publications
Hyperornithinemia-Hyperammonemia-Homocitrullinuria Syndrome in Vietnamese Patients.
Journal: Medicina (Kaunas, Lithuania)
Published: October 17, 2024
Merosin-deficient congenital muscular dystrophy type 1a: detection of LAMA2 variants in Vietnamese patients.
Journal: Frontiers in genetics
Published: March 10, 2023
A novel IGHMBP2 variant and clinical diversity in Vietnamese SMARD1 and CMT2S patients.
Journal: Frontiers in pediatrics
Published: February 14, 2023
In silico validation revealed the role of SCN5A mutations and their genotype-phenotype correlations in Brugada syndrome.
Journal: Molecular genetics & genomic medicine
Published: January 02, 2023
Targeted next-generation sequencing determined a novel SGCG variant that is associated with limb-girdle muscular dystrophy type 2C: A case report.
Journal: Clinical case reports
Published: October 11, 2022
Feasibility of combining short tandem repeats (STRs) haplotyping with preimplantation genetic diagnosis (PGD) in screening for beta thalassemia.
Journal: PloS one
Published: April 16, 2022
Whole exome sequencing analysis in a couple with three children who died prematurely due to carnitine-acylcarnitine translocase deficiency.
Journal: Taiwanese journal of obstetrics & gynecology
Published: July 19, 2021
A case of self-improving collodion ichthyosis in Vietnam.
Journal: Pediatric dermatology
Published: February 28, 2020
Association of the STAT4, CDKN1A, and IRF5 variants with risk of lupus nephritis and renal biopsy classification in patients in Vietnam.
Journal: Molecular genetics & genomic medicine
Published: December 25, 2019
Primary congenital glaucoma in Vietnam: analysis and identification of novel CYP1B1 variants.
Journal: Ophthalmic genetics
Published: June 01, 2019
Last Updated: 09/26/2026