Corrigendum: Case report and literature review: delayed diagnosis of ARCL1B due to a newly reported homozygous mutation c.464A>C p. (Tyr155Ser) in the EFEMP2 gene.

Journal: Frontiers In Genetics
Published:
Abstract

[This corrects the article DOI: 10.3389/fgene.2024.1453195.].

Authors
Lixue Ouyang, Fan Yang, Hongyu Duan, Chuan Wang

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