MITOCHONDRIAL MYOPATHY - A GENETIC-STUDY OF 71 CASES

被引：29
|
作者：
HARDING, AE [1 ]
PETTY, RKH [1 ]
MORGANHUGHES, JA [1 ]
机构：
[1] NATL HOSP,LONDON WC1N 3BG,ENGLAND
来源：
JOURNAL OF MEDICAL GENETICS | 1988年 / 25卷 / 08期
关键词：
D O I：
10.1136/jmg.25.8.528
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
引用
收藏
页码：528 / 535
页数：8
相关论文
共 50 条
  • [1] MITOCHONDRIAL MYOPATHY - A GENETIC-STUDY OF 68 CASES
    HARDING, AE
    PETTY, RKH
    MORGANHUGHES, JA
    MUSCLE & NERVE, 1986, 9 (05) : 179 - 179
  • [2] MITOCHONDRIAL MYOPATHY - A GENETIC-STUDY
    HARDING, AE
    PETTY, RKH
    MORGANHUGHES, JA
    JOURNAL OF MEDICAL GENETICS, 1985, 22 (02) : 138 - 138
  • [3] MYOTUBULAR MYOPATHY - A CLINICAL, PATHOLOGICAL AND GENETIC-STUDY
    HECKMATT, J
    HODES, D
    DUBOWITZ, V
    NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY, 1981, 7 (03) : 248 - 248
  • [4] GENETIC-STUDY OF 6 CASES OF ICHTHYOSIS
    KAPLANIKONICOFF, L
    SLAVUTSKY, I
    KAPLAN, H
    DEMATTEI, AE
    MEDICINA-BUENOS AIRES, 1982, 42 (01) : 50 - 54
  • [5] CONGENITAL CENTRONUCLEAR (MYOTUBULAR) MYOPATHY - A CLINICAL, PATHOLOGICAL AND GENETIC-STUDY IN 8 CHILDREN
    HECKMATT, JZ
    SEWRY, CA
    HODES, D
    DUBOWITZ, V
    BRAIN, 1985, 108 : 941 - 964
  • [6] A MOLECULAR GENETIC-STUDY OF FOCAL HISTOCHEMICAL DEFECTS IN MITOCHONDRIAL ENCEPHALOMYOPATHIES
    HAMMANS, SR
    SWEENEY, MG
    WICKS, DAG
    MORGANHUGHES, JA
    HARDING, AE
    BRAIN, 1992, 115 : 343 - 365
  • [7] NEUROFIBROMATOSIS - A CLINICAL AND GENETIC-STUDY OF 96 CASES IN GOTHENBURG, SWEDEN
    SAMUELSSON, B
    AXELSSON, R
    ACTA DERMATO-VENEREOLOGICA, 1981, : 67 - 71
  • [8] THE RETINAL MANIFESTATIONS OF MITOCHONDRIAL MYOPATHY - A STUDY OF 22 CASES
    MULLIE, MA
    HARDING, AE
    PETTY, RKH
    IKEDA, H
    MORGANHUGHES, JA
    SANDERS, MD
    CANADIAN JOURNAL OF OPHTHALMOLOGY-JOURNAL CANADIEN D OPHTALMOLOGIE, 1985, 20 (02): : 60 - 60
  • [9] THE RETINAL MANIFESTATIONS OF MITOCHONDRIAL MYOPATHY - A STUDY OF 22 CASES
    MULLIE, MA
    HARDING, AE
    PETTY, RKH
    IKEDA, H
    MORGANHUGES, JA
    SANDERS, MD
    ARCHIVES OF OPHTHALMOLOGY, 1985, 103 (12) : 1825 - 1830
  • [10] A CONTRIBUTION TO THE GENETIC-STUDY OF CONGENITAL AFIBRINOGENEMIA - REVIEW OF 12 CASES
    KHALDI, F
    TOUMI, NH
    BOUGUERRA, F
    BOUDICHE, A
    HAFSIA, A
    KHROUF, N
    BENNACEUR, B
    ANNALES DE PEDIATRIE, 1991, 38 (07): : 461 - 467
12345