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Characterization of cytoskeletal and structural effects of INF2 variants causing glomerulopathy and neuropathy.
Sci Rep. 2023 Jul 25;13(1):12003. doi: 10.1038/s41598-023-38588-7.
Sci Rep. 2023.
PMID: 37491439
Free PMC article.
Merosin-deficient congenital muscular dystrophy type 1a: detection of LAMA2 variants in Vietnamese patients.
Tran VK, Nguyen NL, Tran LNT, Le PT, Tran AH, Pham TLA, Lien NTK, Xuan NT, Thanh LT, Ta TV, Tran TH, Nguyen HH.
Tran VK, et al. Among authors: tran lnt.
Front Genet. 2023 Jun 14;14:1183663. doi: 10.3389/fgene.2023.1183663. eCollection 2023.
Front Genet. 2023.
PMID: 37388928
Free PMC article.
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Alopecia and hearing loss in a boy.
Trinh NB, Vu HA, Pham AK, Adawi W, Castillo SA, Tran LNT.
Trinh NB, et al. Among authors: tran lnt.
Pediatr Dermatol. 2021 Nov;38(6):e61-e62. doi: 10.1111/pde.14768.
Pediatr Dermatol. 2021.
PMID: 34931354
No abstract available.
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Spontaneous cerebrospinal fluid leak via foramen rotundum in a non-obese male presented as pseudo-Chiari malformation type I: a case report and literature review.
Luong DH, Chen YC, Tran LNT, Hung SH, Ly QX.
Luong DH, et al. Among authors: tran lnt.
J Int Med Res. 2020 Jun;48(6):300060520924212. doi: 10.1177/0300060520924212.
J Int Med Res. 2020.
PMID: 32571109
Free PMC article.
Review.
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