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Article

Lack of association of the Norrie disease gene with retinoschisis phenotype.

Japanese journal of ophthalmology - 1 Jan 2000

Shastry B S, Hiraoka M, Trese M T

Abstract excerpt

PURPOSE: It has been reported recently that mice carrying a disrupted Norrie disease gene produced alterations in the murine eye that are similar to congenital retinoschisis. Therefore, it was of interest to determine whether mutations in the Norrie disease gene can account for the disease in families with retinoschisis that do not carry mutations in the retinoschisis gene. METHODS: The patient set comprised 5...

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Identifiers

PMID: 11094177
DOI: 10.1016/s0021-5155(00)00288-4

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