Associated Papers
The Landscape of Point Mutations in Human Protein Coding Genes Leading to Pregnancy Loss.
Maksiutenko EM et al.
International Journal of Molecular Sciences, 2023
38139401 (PubMed )
Supplement: ijms-24-17572-s001.zip › Supplementary_Table_S1.xlsx › Sheet1
A Novel De Novo NFKBIA Missense Mutation Associated to Ectodermal Dysplasia with Dysgammaglobulinemia.
Chear CT et al.
Genes, 2022
36292785 (PubMed )
Supplement: genes-13-01900-s001.zip › genes-1944565-supplementary.pdf
Severe influenza pneumonitis in children with inherited TLR3 deficiency.
Lim HK et al.
The Journal of Experimental Medicine, 2019
31217193 (PubMed )
Supplement: JEM_20181621_sm.pdf
Novel genes and mutations in patients affected by recurrent pregnancy loss.
Quintero-Ronderos P et al.
Plos One, 2017
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