MITOCHONDRIAL MYOPATHIES - GENETIC-DEFECTS

被引：17

作者：

HARDING, AE ^{[1
]}

HOLT, IJ ^{[1
]}

COOPER, JM ^{[1
]}

SCHAPIRA, AHV ^{[1
]}

SWEENEY, M ^{[1
]}

CLARK, JB ^{[1
]}

MORGANHUGHES, JA ^{[1
]}

机构：

[1] ST BARTHOLOMEWS HOSP & MED COLL,DEPT BIOCHEM,LONDON EC1M 6BQ,ENGLAND

来源：

BIOCHEMICAL SOCIETY TRANSACTIONS | 1990年 / 18卷 / 04期

关键词：

D O I：

10.1042/bst0180519

中图分类号：

Q5 [生物化学]; Q7 [分子生物学];

学科分类号：

071010 ; 081704 ;

摘要：

引用

页码：519 / 522

页数：4

共 39 条

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[32]

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[34] MITOCHONDRIAL-DNA HETEROPLASMY IN DROSOPHILA-MAURITIANA [J].

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[35]

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[37] MITOCHONDRIAL-DNA MUTATION ASSOCIATED WITH LEBERS HEREDITARY OPTIC NEUROPATHY [J].

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[38]

ZEVIANI M, 1988, NEUROLOGY, V38, P1339

[39] AN AUTOSOMAL DOMINANT DISORDER WITH MULTIPLE DELETIONS OF MITOCHONDRIAL-DNA STARTING AT THE D-LOOP REGION [J].

ZEVIANI, M ;

SERVIDEI, S ;

GELLERA, C ;

BERTINI, E ;

DIMAURO, S ;

DIDONATO, S .

NATURE, 1989, 339 (6222) :309-311

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