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Gene symbol: AGXT. Disease: primary hyperoxaluria type I.
Hum Genet. 1999 May;104(5):441. doi: 10.1007/s004390050984.
Hum Genet. 1999.
PMID: 10394939
No abstract available.
AGXT gene mutations and their influence on clinical heterogeneity of type 1 primary hyperoxaluria.
Amoroso A, Pirulli D, Florian F, Puzzer D, Boniotto M, Crovella S, Zezlina S, Spanò A, Mazzola G, Savoldi S, Ferrettini C, Berutti S, Petrarulo M, Marangella M.
Amoroso A, et al. Among authors: ferrettini c.
J Am Soc Nephrol. 2001 Oct;12(10):2072-2079. doi: 10.1681/ASN.V12102072.
J Am Soc Nephrol. 2001.
PMID: 11562405
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Molecular analysis of hyperoxaluria type 1 in Italian patients reveals eight new mutations in the alanine: glyoxylate aminotransferase gene.
Pirulli D, Puzzer D, Ferri L, Crovella S, Amoroso A, Ferrettini C, Marangella M, Mazzola G, Florian F.
Pirulli D, et al. Among authors: ferrettini c.
Hum Genet. 1999 Jun;104(6):523-5. doi: 10.1007/s004390050998.
Hum Genet. 1999.
PMID: 10453743
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Molecular analysis of the AGXT gene in Italian patients with primary hyperoxaluria type 1 (PH1).
Ferrettini C, Pirulli D, Cosseddu D, Marangella M, Petrarulo M, Mazzola G, Vatta S, Amoroso A.
Ferrettini C, et al.
J Nephrol. 1998 Mar-Apr;11 Suppl 1:18-22.
J Nephrol. 1998.
PMID: 9604804
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