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Zhonghua Yan Ke Za Zhi. 2011 Nov;47(11):1038-42.

[Molecular genetics advances of congenital idiopathic nystagmus].

[Article in Chinese]

Author information

  • 1Clinical College of Ophthalmology of Tianjin Medical University, Tianjin Eye Hospital and Institute, Tianjin Key Laboratory of Ophthalmology and Visual Science, Tianjin 300020, China.

Abstract

Congenital idiopathic nystagmus (CIN) is genetically heterogeneous. Autosomal dominant, autosomal recessive and X-linked patterns of inheritance have described. At least three distinct loci are related to autosomal dominant and X-linked patterns. One causative gene for X-linked form has been identified (FRMD7, Xq26.2) through linkage analysis. The molecular genetics advances of the congenital idiopathic nystagmus (CIN) are reviewed.

PMID:
22336070
[PubMed - indexed for MEDLINE]
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