Chear, C.T.; El Farran, B.A.K.; Sham, M.; Ramalingam, K.; Noh, L.M.; Ismail, I.H.; Chiow, M.Y.; Baharin, M.F.; Ripen, A.M.; Mohamad, S.B.
A Novel De Novo NFKBIA Missense Mutation Associated to Ectodermal Dysplasia with Dysgammaglobulinemia. Genes 2022, 13, 1900.
https://doi.org/10.3390/genes13101900
AMA Style
Chear CT, El Farran BAK, Sham M, Ramalingam K, Noh LM, Ismail IH, Chiow MY, Baharin MF, Ripen AM, Mohamad SB.
A Novel De Novo NFKBIA Missense Mutation Associated to Ectodermal Dysplasia with Dysgammaglobulinemia. Genes. 2022; 13(10):1900.
https://doi.org/10.3390/genes13101900
Chicago/Turabian Style
Chear, Chai Teng, Bader Abdul Kader El Farran, Marina Sham, Kavetha Ramalingam, Lokman Mohd Noh, Intan Hakimah Ismail, Mei Yee Chiow, Mohd Farid Baharin, Adiratna Mat Ripen, and Saharuddin Bin Mohamad.
2022. "A Novel De Novo NFKBIA Missense Mutation Associated to Ectodermal Dysplasia with Dysgammaglobulinemia" Genes 13, no. 10: 1900.
https://doi.org/10.3390/genes13101900
APA Style
Chear, C. T., El Farran, B. A. K., Sham, M., Ramalingam, K., Noh, L. M., Ismail, I. H., Chiow, M. Y., Baharin, M. F., Ripen, A. M., & Mohamad, S. B.
(2022). A Novel De Novo NFKBIA Missense Mutation Associated to Ectodermal Dysplasia with Dysgammaglobulinemia. Genes, 13(10), 1900.
https://doi.org/10.3390/genes13101900