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Year | Number of Results |
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1996 | 1 |
2006 | 1 |
2013 | 1 |
2024 | 0 |
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First case of homozygous C1 inhibitor deficiency.
J Allergy Clin Immunol. 2006 Dec;118(6):1330-5. doi: 10.1016/j.jaci.2006.07.035. Epub 2006 Sep 18.
J Allergy Clin Immunol. 2006.
PMID: 17137866
De novo homozygous mutation of the C1 inhibitor gene in a patient with hereditary angioedema.
Bafunno V, Divella C, Sessa F, Tiscia GL, Castellano G, Gesualdo L, Margaglione M, Montinaro V.
Bafunno V, et al.
J Allergy Clin Immunol. 2013 Sep;132(3):748-750.e3. doi: 10.1016/j.jaci.2013.04.006. Epub 2013 May 17.
J Allergy Clin Immunol. 2013.
PMID: 23688413
No abstract available.
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Exhaustive mutation scanning by fluorescence-assisted mismatch analysis discloses new genotype-phenotype correlations in angiodema.
Verpy E, Biasotto M, Brai M, Misiano G, Meo T, Tosi M.
Verpy E, et al.
Am J Hum Genet. 1996 Aug;59(2):308-19.
Am J Hum Genet. 1996.
PMID: 8755917
Free PMC article.
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