Congenital cataracts: gene mapping

被引：39

作者：

He, WG

Li, SB

机构：

[1] Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA

[2] Univ S Alabama, Dept Med Genet, Mobile, AL 36688 USA

来源：

HUMAN GENETICS | 2000年 / 106卷 / 01期

关键词：

D O I：

10.1007/s004390051002

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

Congenital cataracts are one of the major causes of induced blindness in children. Gene mapping is an important step in understanding the molecular defects of congenital cataracts. Some congenital cataract genes have been mapped, and more genes will be located and identified in the future. The locations and candidate locations of congenital cataract genes are discussed in this review.

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页码：1 / 13

页数：13

相关论文

共 210 条

[71] Marshall syndrome associated with a splicing defect at the COL11A1 locus [J].

Griffith, AJ ;

Sprunger, LK ;

Sirko-Osadsa, DA ;

Tiller, GE ;

Meisler, MH ;

Warman, ML .

AMERICAN JOURNAL OF HUMAN GENETICS, 1998, 62 (04) :816-823

[72]

Grimes PA, 1998, INVEST OPHTH VIS SCI, V39, P1863

[73] INDUCTION OF ECTOPIC EYES BY TARGETED EXPRESSION OF THE EYELESS GENE IN DROSOPHILA [J].

HALDER, G ;

CALLAERTS, P ;

GEHRING, WJ .

SCIENCE, 1995, 267 (5205) :1788-1792

[74] Missense mutations in the most ancient residues of the PAX6 paired domain underlie a spectrum of human congenital eye malformations [J].

Hanson, I ;

Churchill, A ;

Love, J ;

Axton, R ;

Moore, T ;

Clarke, M ;

Meire, F ;

van Heyningen, V .

HUMAN MOLECULAR GENETICS, 1999, 8 (02) :165-172

[75] MUTATIONS AT THE PAX6 LOCUS ARE FOUND IN HETEROGENEOUS ANTERIOR SEGMENT MALFORMATIONS INCLUDING PETERS ANOMALY [J].

HANSON, IM ;

FLETCHER, JM ;

JORDAN, T ;

BROWN, A ;

TAYLOR, D ;

ADAMS, RJ ;

PUNNETT, HH ;

VANHEYNINGEN, V .

NATURE GENETICS, 1994, 6 (02) :168-173

[76]

HARMS WA, 1977, J KANSAS MED SOC, V78, P497

[77] CONFIRMATION OF ASSIGNMENT OF THE HUMAN ALPHA-1-CRYSTALLIN GENE(CRYA1) TO CHROMOSOME 21 WITH REGIONAL LOCALIZATION TO Q22.3 [J].

HAWKINS, JW ;

VANKEUREN, ML ;

PIATIGORSKY, J ;

LAW, ML ;

PATTERSON, D ;

KAO, FT .

HUMAN GENETICS, 1987, 76 (04) :375-380

[78]

HE W, 1999, IN PRESS AM J MED GE

[79] ASSIGNMENT OF THE ZETA-CRYSTALLIN GENE (CRYZ) TO HUMAN-CHROMOSOME 1P22-P-31 AND IDENTIFICATION OF RESTRICTION-FRAGMENT-LENGTH-POLYMORPHISMS [J].

HEINZMANN, C ;

KOJIS, TL ;

GONZALEZ, P ;

RAO, PV ;

ZIGLER, JS ;

POLYMEROPOULOS, MH ;

KLISAK, I ;

SPARKES, RS ;

MOHANDAS, T ;

BATEMAN, JB .

GENOMICS, 1994, 23 (02) :403-407

[80] Gene localization for aculeiform cataract, on chromosome 2q33-35 [J].

Héon, E ;

Liu, S ;

Billingsley, G ;

Bernasconi, O ;

Tsifildis, C ;

Schorderet, DF ;

Munier, FL .

AMERICAN JOURNAL OF HUMAN GENETICS, 1998, 63 (03) :921-926

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