Two new missense mutations (A105T and C110G) in the norrin gene in two Italian families with Norrie disease and familial exudative vitreoretinopathy.

I. Torrente, M. Mangino, M. Gennarelli, G. Novelli, A. Giannotti, P. Vadalà, B. Dallapiccola

Research output: Contribution to journalArticlepeer-review

Original languageEnglish
Pages (from-to)242-244
Number of pages3
JournalAmerican Journal of Medical Genetics
Issue number2
Publication statusPublished - 1997

Cite this