[Albinism. Current clinical and molecular genetic aspects of an important differential congenital nystagmus diagnosis].

作者信息

Lorenz B

机构信息

Abteilung für Pädiatrische Ophthalmologie, Strabismologie und Ophthalmogenetik in der Klinik und Poliklinik für Augenheilkunde der Universität Regensburg.

出版信息

Ophthalmologe. 1997 Jul;94(7):534-44. doi: 10.1007/s003470050155.

DOI:10.1007/s003470050155

PMID:9333404

Abstract

摘要

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引用本文的文献

[Abnormal representations in the visual cortex of patients with albinism: diagnostic aid and model for the investigation of the self-organisation of the visual cortex].[白化病患者视觉皮层的异常表现：视觉皮层自组织研究的诊断辅助与模型]

Ophthalmologe. 2007 Aug;104(8):666-73. doi: 10.1007/s00347-007-1589-7.

Monocular visual activation patterns in albinism as revealed by functional magnetic resonance imaging.功能磁共振成像揭示的白化病单眼视觉激活模式

Hum Brain Mapp. 2004 Sep;23(1):40-52. doi: 10.1002/hbm.20046.

Deletion in the OA1 gene in a family with congenital X linked nystagmus.一个患有先天性X连锁眼球震颤的家族中OA1基因的缺失。

Br J Ophthalmol. 2001 Sep;85(9):1098-103. doi: 10.1136/bjo.85.9.1098.

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