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

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 journal › Article › peer-review

Original language	English
Pages (from-to)	242-244
Number of pages	3
Journal	American Journal of Medical Genetics
Volume	72
Issue number	2
Publication status	Published - 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 journal › Article › peer-review

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AU - Torrente, I.

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AU - Gennarelli, M.

AU - Novelli, G.

AU - Giannotti, A.

AU - Vadalà, P.

AU - Dallapiccola, B.

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

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