Ouyang, L., Ouyang, L., Ouyang, L., Yang, F., Yang, F., Duan, H., . . . Wang, C. (2024, December). 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. Frontiers in Genetics.
Chicago Style (17th ed.) CitationOuyang, Lixue, et al. "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." Frontiers in Genetics Dec. 2024.
MLA (9th ed.) CitationOuyang, Lixue, et al. "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." Frontiers in Genetics, Dec. 2024.
Warning: These citations may not always be 100% accurate.