MITOCHONDRIAL-DNA POLYMORPHISM IN FINNISH FAMILIES WITH LEBERS HEREDITARY OPTIC NEURORETINOPATHY

被引：23

作者：

VILKKI, J

SAVONTAUS, ML

KALIMO, H

NIKOSKELAINEN, EK

机构：

[1] UNIV TURKU,INST BIOMED,DEPT MED GENET,SF-20520 TURKU 52,FINLAND

[2] UNIV TURKU,DEPT BIOL,SF-20520 TURKU 52,FINLAND

[3] UNIV TURKU,DEPT PATHOL,SF-20520 TURKU 52,FINLAND

[4] UNIV TURKU,CENT HOSP,DEPT OPHTHALMOL,SF-20520 TURKU 52,FINLAND

来源：

关键词：

D O I：

10.1007/BF00291155

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：208 / 212

页数：5

共 18 条

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NIKOSKELAINEN, EK
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WANNE, OP
KATILA, MJ
NUMMELIN, KU
[J]. ARCHIVES OF OPHTHALMOLOGY, 1987, 105 (05) : 665 - 671
[14] SEEDORFF T, 1985, ACTA OPHTHALMOL, V63, P135
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UEMURA, A
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OHBA, N
[J]. BRITISH JOURNAL OF OPHTHALMOLOGY, 1987, 71 (07) : 531 - 536
[16] VAN SENUS A. H. C., 1963, DOC OPHTHALMOL, V17, P1
[17] HUMAN MITOCHONDRIAL-DNA TYPES IN FINLAND
VILKKI, J
SAVONTAUS, ML
NIKOSKELAINEN, EK
[J]. HUMAN GENETICS, 1988, 80 (04) : 317 - 321
[18] WALLACE DC, 1970, AUST ANN MED, V19, P1