Merosin-deficient congenital muscular dystrophy type 1a: detection of LAMA2 variants in Vietnamese patients.

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Bibliographic Details
Title: Merosin-deficient congenital muscular dystrophy type 1a: detection of LAMA2 variants in Vietnamese patients.
Authors: Tran VK; Center for Gene and Protein Research, Hanoi Medical University, Hanoi, Vietnam., Nguyen NL; Institute of Genome Research, Vietnam Academy of Science and Technology (VAST), Hanoi, Vietnam., Tran LNT; Center for Gene and Protein Research, Hanoi Medical University, Hanoi, Vietnam., Le PT; Center for Gene and Protein Research, Hanoi Medical University, Hanoi, Vietnam., Tran AH; Center for Gene and Protein Research, Hanoi Medical University, Hanoi, Vietnam., Pham TLA; Center for Gene and Protein Research, Hanoi Medical University, Hanoi, Vietnam., Lien NTK; Institute of Genome Research, Vietnam Academy of Science and Technology (VAST), Hanoi, Vietnam., Xuan NT; Institute of Genome Research, Vietnam Academy of Science and Technology (VAST), Hanoi, Vietnam., Thanh LT; Institute of Genome Research, Vietnam Academy of Science and Technology (VAST), Hanoi, Vietnam., Ta TV; Center for Gene and Protein Research, Hanoi Medical University, Hanoi, Vietnam.; Hanoi Medical University Hospital, Hanoi Medical University, Hanoi, Vietnam., Tran TH; Center for Gene and Protein Research, Hanoi Medical University, Hanoi, Vietnam.; Hanoi Medical University Hospital, Hanoi Medical University, Hanoi, Vietnam., Nguyen HH; Institute of Genome Research, Vietnam Academy of Science and Technology (VAST), Hanoi, Vietnam.; Graduate University of Science and Technology, Vietnam Academy of Science and Technology (VAST), Hanoi, Vietnam.
Source: Frontiers in genetics [Front Genet] 2023 Jun 14; Vol. 14, pp. 1183663. Date of Electronic Publication: 2023 Jun 14 (Print Publication: 2023).
Publication Type: Journal Article
Journal Info: Publisher: Frontiers Research Foundation Country of Publication: Switzerland NLM ID: 101560621 Publication Model: eCollection Cited Medium: Print ISSN: 1664-8021 (Print) Linking ISSN: 16648021 NLM ISO Abbreviation: Front Genet Subsets: PubMed not MEDLINE
Database: MEDLINE Ultimate
Description
ISSN:1664-8021
DOI:10.3389/fgene.2023.1183663