LEBERS HEREDITARY OPTIC NEUROPATHY - THE CLINICAL RELEVANCE OF DIFFERENT MITOCHONDRIAL-DNA MUTATIONS

被引：98

作者：

RIORDANEVA, P ^{[1
]}

HARDING, AE ^{[1
]}

机构：

[1] UNIV LONDON, INST NEUROL, DEPT CLIN NEUROL, NEUROGENET SECT, LONDON WC1N 3BG, ENGLAND

来源：

JOURNAL OF MEDICAL GENETICS | 1995年 / 32卷 / 02期

关键词：

D O I：

10.1136/jmg.32.2.81

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

[No abstract available]

引用

页码：81 / 87

页数：7

共 71 条

[1] FURTHER CLINICAL AND PATHOLOGICAL OBSERVATIONS ON LEBERS OPTIC ATROPHY [J].

ADAMS, JH ;

BLACKWOOD, W ;

WILSON, J .

BRAIN, 1966, 89 :15-+

[2] RAPID SHIFT IN GENOTYPE OF HUMAN MITOCHONDRIAL-DNA IN A FAMILY WITH LEBER HEREDITARY OPTIC NEUROPATHY [J].

BOLHUIS, PA ;

BLEEKERWAGEMAKERS, EM ;

PONNE, NJ ;

VANSCHOONEVELD, MJ ;

WESTERVELD, A ;

VANDENBOGERT, C ;

TABAK, HF .

BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1990, 170 (03) :994-997

[3]

BROWN MD, 1992, AM J HUM GENET, V51, P378

[4]

BROWN MD, 1994, AM J HUM GENET, V55, P410

[5] LEBERS HEREDITARY OPTIC NEUROPATHY MASQUERADING AS TOBACCO-ALCOHOL AMBLYOPIA [J].

CULLOM, ME ;

HEHER, KL ;

MILLER, NR ;

SAVINO, PJ ;

JOHNS, DR .

ARCHIVES OF OPHTHALMOLOGY, 1993, 111 (11) :1482-1485

[6]

ERIKSON RP, 1972, AM J HUM GENET, V24, P348

[7] ASSOCIATION OF THE 11778 MITOCHONDRIAL-DNA MUTATION AND DEMYELINATING DISEASE [J].

FLANIGAN, KM ;

JOHNS, DR .

NEUROLOGY, 1993, 43 (12) :2720-2722

[8] MITOCHONDRIAL ENCEPHALOPATHIES - MOLECULAR GENETIC DIAGNOSIS FROM BLOOD-SAMPLES [J].

HAMMANS, SR ;

SWEENEY, MG ;

BROCKINGTON, M ;

MORGANHUGHES, JA ;

HARDING, AE .

LANCET, 1991, 337 (8753) :1311-1313

[9] OCCURRENCE OF A MULTIPLE SCLEROSIS-LIKE ILLNESS IN WOMEN WHO HAVE A LEBERS HEREDITARY OPTIC NEUROPATHY MITOCHONDRIAL-DNA MUTATION [J].

HARDING, AE ;

SWEENEY, MG ;

MILLER, DH ;

MUMFORD, CJ ;

KELLARWOOD, H ;

MENARD, D ;

MCDONALD, WI ;

COMPSTON, DAS .

BRAIN, 1992, 115 :979-989

[10]

HARDING SE, 1994, MITOCHONDRIAL DISORD

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