Homogeneity of kerato-epithelin codon 124 mutations in Japanese patients with either of two types of corneal stromal dystrophy

被引：44

作者：

Mashima, Y

Imamura, Y

Konishi, M

Nagasawa, A

Yamada, M

Oguchi, Y

Kudoh, J

Shimizu, N

机构：

[1] Keio Univ, Sch Med, Dept Ophthalmol, Shinjuku Ku, Tokyo 160, Japan

[2] Keio Univ, Sch Med, Dept Mol Biol, Shinjuku Ku, Tokyo 160, Japan

来源：

AMERICAN JOURNAL OF HUMAN GENETICS | 1997年 / 61卷 / 06期

关键词：

D O I：

10.1086/301649

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：1448 / 1450

页数：3

共 19 条

[1]

AKIYA S, 1970, Archives of Ophthalmology, V84, P179

[2] PHYLOGENETIC ANALYSIS OF LEBERS HEREDITARY OPTIC NEUROPATHY MITOCHONDRIAL DNAS INDICATES MULTIPLE INDEPENDENT OCCURRENCES OF THE COMMON MUTATIONS [J].

BROWN, MD ;

TORRONI, A ;

RECKORD, CL ;

WALLACE, DC .

HUMAN MUTATION, 1995, 6 (04) :311-325

[3] THE RELATIONSHIP BETWEEN GRANULAR, LATTICE TYPE-1, AND AVELLINO CORNEAL DYSTROPHIES - A HISTOPATHOLOGIC STUDY [J].

FOLBERG, R ;

STONE, EM ;

SHEFFIELD, VC ;

MATHERS, WD .

ARCHIVES OF OPHTHALMOLOGY, 1994, 112 (08) :1080-1085

[4]

FOLBERG R, 1988, OPHTHALMOLOGY, V95, P46

[5] A HOMOZYGOUS 1-BASE PAIR DELETION IN THE ARRESTIN GENE IS A FREQUENT CAUSE OF OGUCHI DISEASE IN JAPANESE [J].

FUCHS, S ;

NAKAZAWA, M ;

MAW, M ;

TAMAI, M ;

OGUCHI, Y ;

GAL, A .

NATURE GENETICS, 1995, 10 (03) :360-362

[6] HISTOCHEMISTRY OF CORNEAL GRANULAR DYSTROPHY [J].

GARNER, A .

BRITISH JOURNAL OF OPHTHALMOLOGY, 1969, 53 (12) :799-&

[7] GENETIC REFINEMENT OF THE CHROMOSOME-5Q LATTICE CORNEAL-DYSTROPHY TYPE-I LOCUS TO WITHIN A 2-CM INTERVAL [J].

GREGORY, CY ;

EVANS, K ;

BHATTACHARYA, SS .

JOURNAL OF MEDICAL GENETICS, 1995, 32 (03) :224-226

[8] UNUSUAL SUPERFICIAL VARIANT OF GRANULAR DYSTROPHY OF CORNEA [J].

HADDAD, R ;

FONT, RL ;

FINE, BS .

AMERICAN JOURNAL OF OPHTHALMOLOGY, 1977, 83 (02) :213-218

[9]

HOLLAND EJ, 1992, OPHTHALMOLOGY, V99, P1564

[10]

HOWELL N, 1995, GENETICS, V140, P285

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