DETECTION OF PLATELET MITOCHONDRIAL-DNA DELETIONS IN KEARNS-SAYRE SYNDROME

被引:0
|
作者
OTA, Y
AWAYA, S
TANAKA, M
OZAWA, T
机构
[1] NAGOYA UNIV,SCH MED,DEPT OPHTHALMOL,NAGOYA,AICHI 466,JAPAN
[2] NAGOYA UNIV,SCH MED,DEPT BIOMED CHEM,NAGOYA,AICHI 466,JAPAN
关键词
D O I
暂无
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
引用
收藏
页码:1137 / 1137
页数:1
相关论文
共 50 条
  • [21] DETECTION OF PLATELET MITOCHONDRIAL-DNA DELETIONS IN KEARNS-SAYRE-SYNDROME (VOL 32, PG 2668, 1994)
    OTA, Y
    TANAKA, M
    SATO, W
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 1995, 36 (01) : 3 - 3
  • [22] NOVEL 2905-BP MITOCHONDRIAL-DNA DELETION IN KEARNS-SAYRE SYNDROME
    BECHER, MW
    NOLL, WW
    HURKO, O
    PRICE, DL
    JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 1995, 54 (03): : 453 - 453
  • [23] 3.1-KB DELETION OF MITOCHONDRIAL-DNA IN A PATIENT WITH KEARNS-SAYRE SYNDROME
    KLOPSTOCK, T
    BISCHOF, F
    GEROK, K
    DEUSCHL, G
    SEIBEL, P
    KETELSEN, UP
    REICHMANN, H
    ACTA NEUROPATHOLOGICA, 1995, 90 (02) : 126 - 129
  • [24] NO MATERNAL TRANSMISSION OF DELETED MITOCHONDRIAL-DNA TO A CHILD OF A WOMAN WITH KEARNS-SAYRE SYNDROME
    LARSSON, NG
    EIKEN, HG
    BOMAN, H
    HOLME, E
    OLDFORS, A
    TULINIUS, M
    AMERICAN JOURNAL OF HUMAN GENETICS, 1991, 49 (04) : 46 - 46
  • [25] LEBERS HEREDITARY OPTIC NEUROPATHY AND KEARNS-SAYRE SYNDROME - MITOCHONDRIAL-DNA MUTATIONS
    PHILLIPS, CI
    GOSDEN, CM
    SURVEY OF OPHTHALMOLOGY, 1991, 35 (06) : 463 - 472
  • [26] Kearns-Sayre syndrome with a novel mitochondrial DNA deletion
    Marin-Garcia, J
    Goldenthal, MJ
    Sarnat, HB
    JOURNAL OF CHILD NEUROLOGY, 2000, 15 (08) : 555 - 558
  • [27] CHARACTERIZATION OF A 5025-BASE-PAIR MITOCHONDRIAL-DNA DELETION IN KEARNS-SAYRE SYNDROME
    VAZQUEZACEVEDO, M
    CORIA, R
    GONZALEZASTIAZARAN, A
    MEDINACRESPO, V
    RIDAURASANZ, C
    GONZALEZHALPHEN, D
    BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, 1995, 1271 (2-3): : 363 - 368
  • [28] DELETION OF MITOCHONDRIAL-DNA IN THE ENDOMYOCARDIAL BIOPSY SAMPLE FROM A PATIENT WITH KEARNS-SAYRE SYNDROME
    ANAN, R
    NAKAGAWA, M
    HIGUCHI, I
    NAKAO, S
    NOMOTO, K
    TANAKA, H
    EUROPEAN HEART JOURNAL, 1992, 13 (12) : 1718 - 1719
  • [29] INSITU HYBRIDIZATION OF MITOCHONDRIAL-DNA IN THE HEART OF A PATIENT WITH KEARNS-SAYRE SYNDROME AND DILATATIVE CARDIOMYOPATHY
    MULLERHOCKER, J
    SEIBEL, P
    SCHNEIDERBANGER, K
    ZIETZ, C
    OBERMAIERKUSSER, B
    GERBITZ, KD
    KADENBACH, B
    HUMAN PATHOLOGY, 1992, 23 (12) : 1431 - 1437
  • [30] MITOCHONDRIAL CARDIOMYOPATHY IN KEARNS-SAYRE SYNDROME
    KLEBER, FX
    PARK, JW
    JOHANNES, A
    HUBNER, G
    KONIG, E
    ZEITSCHRIFT FUR KARDIOLOGIE, 1986, 75 : 11 - 11