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 journalArticle

18 Citations (Scopus)
Original languageEnglish
Pages (from-to)242-244
Number of pages3
JournalAmerican Journal of Medical Genetics
Volume72
Issue number2
Publication statusPublished - 1997

Cite this

Two new missense mutations (A105T and C110G) in the norrin gene in two Italian families with Norrie disease and familial exudative vitreoretinopathy. / Torrente, I.; Mangino, M.; Gennarelli, M.; Novelli, G.; Giannotti, A.; Vadalà, P.; Dallapiccola, B.

In: American Journal of Medical Genetics, Vol. 72, No. 2, 1997, p. 242-244.

Research output: Contribution to journalArticle

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AU - Torrente, I.

AU - Mangino, M.

AU - Gennarelli, M.

AU - Novelli, G.

AU - Giannotti, A.

AU - Vadalà, P.

AU - Dallapiccola, B.

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JF - American Journal of Medical Genetics, Part A

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