Cui Qingyang, Wang Mengbin, Cao Yinli, Tang Chenghe. A case report and literature review on severe combined immunodeficiency caused by new mutation of RAG1 gene[J]. Clinical Focus, 2022, 37(2): 155-161.
Diamond CD, Sanchez MJ, LaBelle JL. Diagnostic criteria and evaluation of severe combined immunodeficiency in the neonate[J]. Pediatr Ann, 2015,44(7):e181-7.
[2]
Kwan A, Abraham RS, Currier R, et al. Newborn screening for severe combined immunodeficiency in 11 screening programs in the United States[J]. JAMA, 2014,312(7):729-738.
doi: 10.1001/jama.2014.9132URL
Cirillo E, Giardino G, Gallo V, et al. Severe Combined Immunodeficiency--An Update[J]. Ann N Y Acad Sci, 2015,1356(1):90-106.
doi: 10.1111/nyas.12849URL
[5]
Kelly BT, Tam JS, Verbsky JW, et al. Screening for severe combined immunodeficiency in neonates[J]. Clin Epidemiol, 2013,5:363-369.
[6]
Buelow BJ, Routes JM, Verbsky JW. Newborn screening for SCID: Where are we now?[J]. Expert Rev Clin Immunol, 2014,10(12):1649-1657.
doi: 10.1586/1744666X.2014.980816URL
[7]
Richards S, Aziz N, Bale S, et al. Standards and guidelines for the interpretation of sequence variants: A joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology[J]. Genet Med, 2015,17(5):405-424.
doi: 10.1038/gim.2015.30
pmid: 25741868
[8]
Lieber MR. The mechanism of double-strand DNA break repair by the nonhomologous DNA end-joining pathway[J]. Annu Rev Biochem, 2010,79:181-211.
doi: 10.1146/biochem.2010.79.issue-1URL