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Page 1
New SLC12A3 disease causative mutation of Gitelman's syndrome.
World J Nephrol. 2016 Nov 6;5(6):551-555. doi: 10.5527/wjn.v5.i6.551.
World J Nephrol. 2016.
PMID: 27872838
Free PMC article.
A Familial Form of Epidermolysis Bullosa Simplex Associated with a Pathogenic Variant in KRT5.
Paduano F, Colao E, Grillone T, Vismara MFM, Amato R, Nisticò S, Mignogna C, Dastoli S, Fabiani F, Zucco R, Trapasso F, Perrotti N, Iuliano R.
Paduano F, et al. Among authors: grillone t.
Genes (Basel). 2021 Sep 25;12(10):1503. doi: 10.3390/genes12101503.
Genes (Basel). 2021.
PMID: 34680898
Free PMC article.
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Novel Mutation in the CHRDL1 Gene Detected in Patients With Megalocornea.
Mangialavori D, Colao E, Carnevali A, Bruzzichessi D, Grillone T, Perrotti N, Iuliano R, Scorcia V.
Mangialavori D, et al. Among authors: grillone t.
Cornea. 2015 Aug;34(8):976-9. doi: 10.1097/ICO.0000000000000472.
Cornea. 2015.
PMID: 26020825
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UMG Lenti: novel lentiviral vectors for efficient transgene- and reporter gene expression in human early hematopoietic progenitors.
Chiarella E, Carrà G, Scicchitano S, Codispoti B, Mega T, Lupia M, Pelaggi D, Marafioti MG, Aloisio A, Giordano M, Nappo G, Spoleti CB, Grillone T, Giovannone ED, Spina R, Bernaudo F, Moore MA, Bond HM, Mesuraca M, Morrone G.
Chiarella E, et al. Among authors: grillone t.
PLoS One. 2014 Dec 12;9(12):e114795. doi: 10.1371/journal.pone.0114795. eCollection 2014.
PLoS One. 2014.
PMID: 25502183
Free PMC article.
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