Merosin-deficient congenital muscular dystrophy type 1a: detection of LAMA2 variants in Vietnamese patients by Van Khanh Tran, Ngoc-Lan Nguyen, Lan Ngoc Thi Tran, Phuong Thi Le, Anh Hai Tran, Tuan L. A. Pham, Nguyen Thi Kim Lien, Nguyen Thi Xuan, Le Tat Thanh, Thanh Van Ta, Thanh Van Ta, Thinh Huy Tran, Thinh Huy Tran, Huy-Hoang Nguyen, Huy-Hoang Nguyen

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A novel IGHMBP2 variant and clinical diversity in Vietnamese SMARD1 and CMT2S patients by Van Khanh Tran, Van Khanh Tran, My Ha Cao, Thi Thanh Hai Nguyen, Phuong Thi Le, Hai Anh Tran, Dung Chi Vu, Ha Thu Nguyen, Mai Thi Phương Nguyen, The-Hung Bui, The-Hung Bui, Thanh Binh Nguyen, Thanh Van Ta, Thanh Van Ta, Thinh Huy Tran, Thinh Huy Tran

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Molecular Characterization and Genotype-Phenotype Correlation of G6PD Mutations in Five Ethnicities of Northern Vietnam by Thi Thao Ngo, Thinh Huy Tran, Thanh Dat Ta, Thi Phuong Le, Phuoc Dung Nguyen, Mai Anh Tran, The-Hung Bui, Thanh Van Ta, Van Khanh Tran

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Targeted next‐generation sequencing determined a novel SGCG variant that is associated with limb‐girdle muscular dystrophy type 2C: A case report by Nam‐Chung Tran, Tuan Anh Nguyen, Thanh Dat Ta, Thinh Huy Tran, Phuoc‐Dung Nguyen, Chi Dung Vu, Van‐Hung Nguyen, The‐Hung Bui, Thanh Van Ta, Van Khanh Tran

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Association of the STAT4, CDKN1A, and IRF5 variants with risk of lupus nephritis and renal biopsy classification in patients in Vietnam by Trung Dung Nghiem, Gia Tuyen Do, Long Hoang Luong, Quy Linh Nguyen, Ha Viet Dang, Anh Nguyen Viet, Thuy Thu Nguyen, Van Khanh Tran, Thanh Van Ta, Thinh Huy Tran

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Feasibility of combining short tandem repeats (STRs) haplotyping with preimplantation genetic diagnosis (PGD) in screening for beta thalassemia. by Vu Viet Ha Vuong, Thinh Huy Tran, Phuoc-Dung Nguyen, Nha Nguyen Thi, Phuong Le Thi, Dang Thi Minh Nguyet, Manh-Ha Nguyen, The-Hung Bui, Thanh Van Ta, Van-Khanh Tran

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In silico validation revealed the role of SCN5A mutations and their genotype–phenotype correlations in Brugada syndrome by Hung Manh Pham, Duy Phuong Dang, Thanh Dat Ta, Thi Phuong Le, Dinh Phong Phan, Hoai An Trinh, Tuan Viet Tran, Thi Lan Anh Luong, Ha Minh Nguyen, The‐Hung Bui, Thinh Huy Tran, Thanh Van Ta, Van‐Khanh Tran

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The Impact of Vaccination on COVID-19 Outcomes in Vietnam by Ngoc-Lan Thi Nguyen, Hien Thi Thu Nguyen, Vang Le-Quy, Thu-Ba To, Huy Thinh Tran, Tuan Duc Nguyen, Yen Hoang, Anh-Thu Nguyen, Lan Thi Phuong Dam, Nhat-Linh Nguyen, Anh Tuan Dinh-Xuan, Thanh-Van Ta

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Application of short tandem repeats (STRs) in the preimplantation genetic diagnosis (PGD) of α-thalassemia by Vu Viet Ha Vuong, Phuoc-Dung Nguyen, Nha Nguyen Thi, Phuong Le Thi, Dang Thi Minh Nguyet, Manh Ha Nguyen, Hai Anh Tran, Nhat-Minh Dang-Tran, The-Hung Bui, Thinh Huy Tran, Thanh Van Ta, Van-Khanh Tran

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Hyperornithinemia–Hyperammonemia–Homocitrullinuria Syndrome in Vietnamese Patients by Khanh Ngoc Nguyen, Van Khanh Tran, Ngoc Lan Nguyen, Thi Bich Ngoc Can, Thi Kim Giang Dang, Thu Ha Nguyen, Thi Thanh Mai Do, Le Thi Phuong, Thinh Huy Tran, Thanh Van Ta, Nguyen Huu Tu, Chi Dung Vu

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Mutation spectrum of retinoblastoma patients in Vietnam by Dao Nguyen Ha Linh, Nguyen Van Huy, Phuoc‐Dung Nguyen, Phuong Le Thi, Hoang Anh Tuan, Trong Van Nguyen, Thu Ha Tran, Hai Anh Tran, Thanh Dat Ta, Tuan L. A. Pham, The‐Hung Bui, Thinh Huy Tran, Thanh Van Ta, Van‐Khanh Tran

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Case Report: Novel rare mutation c.6353C > G in the ABCA12 gene causing harlequin ichthyosis identified by whole exome sequencing by Van Khanh Tran, Quang Minh Diep, Qiu Zilong, Le Thi Phuong, Hai Anh Tran, Nguyen Van Tung, Nguyen Van Tung, Nguyen Thi Kim Lien, Nguyen Thi Xuan, Le Thi Ha, Thanh Van Ta, Thinh Huy Tran, Nguyen Huy Hoang, Nguyen Huy Hoang

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