APA (7th ed.) Citation

LT, P., WQ, W., SS, H., M, L., SY, Y., DY, K., . . . JC, X. (2026). A Novel Frameshift Variant c.1023_1029del (p.Asp342ArgfsTer54) Leading to Extended Incorrect Protein C Termini in HOMER2 Causing Autosomal Dominant Nonsyndromic Hearing Loss. Journal of clinical laboratory analysis, 40(1), e70137. https://doi.org/10.1002/jcla.70137

Chicago Style (17th ed.) Citation

LT, Peng, et al. "A Novel Frameshift Variant C.1023_1029del (p.Asp342ArgfsTer54) Leading to Extended Incorrect Protein C Termini in HOMER2 Causing Autosomal Dominant Nonsyndromic Hearing Loss." Journal of Clinical Laboratory Analysis 40, no. 1 (2026): e70137. https://doi.org/10.1002/jcla.70137.

MLA (9th ed.) Citation

LT, Peng, et al. "A Novel Frameshift Variant C.1023_1029del (p.Asp342ArgfsTer54) Leading to Extended Incorrect Protein C Termini in HOMER2 Causing Autosomal Dominant Nonsyndromic Hearing Loss." Journal of Clinical Laboratory Analysis, vol. 40, no. 1, 2026, p. e70137, https://doi.org/10.1002/jcla.70137.