3 results for author:"Ferrettini C." in Literature citations
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| 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., Spano A., Mazzola G., Savoldi S. et al. J. Am. Soc. Nephrol. 12:2072-2079(2001) · Mapped (8) |
| 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. Hum. Genet. 104:523-525(1999) · UniProtKB (1) |
| Gene symbol: AGXT. Disease: primary hyperoxaluria type I. Amoroso A., Pirulli D., Puzzer D., Ferri L., Crovella S., Ferrettini C., Marangella M., Mazzola G., Florian F. Hum. Genet. 104:441-441(1999) · UniProtKB (1) |