DEL variants: review of molecular mechanisms, clinical consequences and molecular testing strategy
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics,General Medicine
Link
https://link.springer.com/content/pdf/10.1007/s10142-023-01249-z.pdf
Reference99 articles.
1. Adzhubei IA, Schmidt S, Peshkin L et al (2010) A method and server for predicting damaging missense mutations. Nat Methods 7:248–249. https://doi.org/10.1038/nmeth0410-248
2. Borgmann DM, Mayr S, Polin H et al (2016) Single Molecule fluorescence microscopy and machine learning for rhesus D antigen classification. Sci Rep 6:32317. https://doi.org/10.1038/srep32317
3. Chen DP, Sun CF, Ning HC, Wang WT, Tseng CP (2016) Comprehensive analysis of RHD splicing transcripts reveals the molecular basis for the weak anti-D reactivity of Del -red blood cells. Transfus Med 26:123–129. https://doi.org/10.1111/tme.12270
4. Chen JC, Lin TM, Chen YL, Wang YH, Jin YT, Yue CT (2004) RHD 1227A is an important genetic marker for RhD(el) individuals. Am J Clin Pathol 122:193–198. https://doi.org/10.1309/3XMF-2NV5-707T-JE7X
5. Chen Q, Flegel WA (2005) Random survey for RHD alleles among D+ European persons. Transfusion 45:1183–1191. https://doi.org/10.1111/j.1537-2995.2005.00181.x
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