Elucidating the molecular genetic defect in a family with X-linked congenital nystagmus associated with macular hypoplasia

Preising, M. N. and Op de Laak, J. P. and Sendtner, R. and Funck, S. and Lorenz, B. (2000) Elucidating the molecular genetic defect in a family with X-linked congenital nystagmus associated with macular hypoplasia. In: Association for Research in Vision and Ophthalmology - Annual Meeting 2000, April 30 - May 5, 2000, Fort Lauderdale, Florida.

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Item Type: Conference or Workshop Item (Poster)
Additional Information: Band lag vor /gup
Subjects: 600 Technology > 610 Medical sciences Medicine
Divisions: Medicine > Abteilung für Pädiatrische Ophthalmologie, Strabismologie und Ophthalmogenetik
Depositing User: Petra Gürster
Date Deposited: 13 Oct 2021 04:50
Last Modified: 13 Oct 2021 04:50
URI: https://pred.uni-regensburg.de/id/eprint/42748

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