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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)

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Antonio Pizzuti

Ospedale Casa Sollievo della Sofferenza and Istituto CSS-Mendel

Italy

[email]@css-mendel.it

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Affiliations

Ospedale Casa Sollievo della Sofferenza and Istituto CSS-Mendel, Italy. 2004
Dipartimento di Medicina Sperimentale e Patologia, Università di Roma La Sapienza and Ospedale Casa Sollievo della Sofferenza San Giovanni Rotondo IRCSS, Istituto Mendel, Italy. 2003
Dipartimento di Medicina Sperimentale e Patologia, Università di Roma La Sapienza, Italy. 2003

References

A homozygous GJA1 gene mutation causes a Hallermann-Streiff/ODDD spectrum phenotype. Pizzuti, A., Flex, E., Mingarelli, R., Salpietro, C., Zelante, L., Dallapiccola, B. Hum. Mutat. (2004) [Pubmed]
Epilepsy with auditory features: a LGI1 gene mutation suggests a loss-of-function mechanism. Pizzuti, A., Flex, E., Di Bonaventura, C., Dottorini, T., Egeo, G., Manfredi, M., Dallapiccola, B., Giallonardo, A.T. Ann. Neurol. (2003) [Pubmed]
Mutations of ZFPM2/FOG2 gene in sporadic cases of tetralogy of Fallot. Pizzuti, A., Sarkozy, A., Newton, A.L., Conti, E., Flex, E., Digilio, M.C., Amati, F., Gianni, D., Tandoi, C., Marino, B., Crossley, M., Dallapiccola, B. Hum. Mutat. (2003) [Pubmed]