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PMID: 12607114 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Genetic linkage of Francois-Neetens fleck (mouchetée) corneal dystrophy to chromosome 2q35.

Human genetics ·Vol. 112 ·No. 5-6 ·2003-05-00 ·页码 593-9

Jiao X, Munier FL, Schorderet DF, Zografos L, Smith J, Rubin B, Hejtmancik JF

Abstract

Francois-Neetens fleck (mouchetée) corneal dystrophy is an autosomal dominant corneal dystrophy characterized by scattered small white flecks occurring at all levels of the corneal stroma. We report linkage of the CFD locus to D2S2289 (Z(max)=4.46, theta=0), D2S325 (Z(max)=3.28, theta=0), D2S317 (Z(max)=3.1, theta=0), D2S143 (Z(max)=3.8, theta=0.03), and D2S2382 (Z(max)=5.0, theta=0) on chromosome 2q35. Multipoint analysis confirmed linkage to the region between D2S117 and D2S126 with a maximum multipoint lod score of 5.0 located midway between D2S2289 and D2S325. Analysis of CFD in these same families assuming a 90% penetrance increased the maximum lod score to 6.28 at D2S157.

MeSH 主题词
Chromosome Mapping Chromosomes, Human, Pair 2 Corneal Dystrophies, Hereditary/etiology,genetics Female Genetic Linkage Haplotypes Humans Male Penetrance
作者与单位
共 7 位作者,点击展开单位 / ORCID
Jiao Xiaodong
Ophthalmic Genetics and Clinical Services Branch, National Eye Institute, Bethesda, Maryland 20892-1860, USA.
Munier Francis L
Schorderet Daniel F
Zografos Leonidas
Smith Janine
Rubin Benjamin
Hejtmancik J Fielding
Article Info
Journal
Human genetics
Abbr.
Hum Genet
ISSN
0340-6717
Published
2003-05-00
电子出版
2003-00-27
页码
593-9
Language
English
Country/Region
Germany
NLM ID
7613873
数据资源
OMIM
121850
Analysis Services
Analysis Services

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