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Case Report: A child with NFKB1 haploinsufficiency explaining the linkage between immunodeficiency and short stature
We report the case of a patient with common variable immunodeficiency (CVID) presenting with short stature and treated with recombinant human growth hormone (rhGH). Whole exome sequencing revealed a novel single-nucleotide duplication in the NFKB1 gene (c.904dup, p.Ser302fs), leading to a frameshift...
Autores principales: | Ricci, S., Abu-Rumeileh, S., Campagna, N., Barbati, F., Stagi, S., Canessa, C., Lodi, L., Palterer, B., Maggi, L., Matucci, A., Vultaggio, A., Annunziato, F., Azzari, C. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10434558/ https://www.ncbi.nlm.nih.gov/pubmed/37600787 http://dx.doi.org/10.3389/fimmu.2023.1224603 |
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