NONISOTOPIC AND SENSITIVE METHOD FOR DIAGNOSIS OF MATERNALLY-INHERITED DIABETES AND DEAFNESS

被引：9

作者：

BLANCHE, H ^{[1
]}

FROGUEL, P ^{[1
]}

DAUSSET, J ^{[1
]}

COHEN, D ^{[1
]}

COHEN, N ^{[1
]}

机构：

[1] CTR ETUD POLYMORPHISME HUMAIN,FDN JEAN DAUSSET,CTR HUMAN POLYMORPHISM STUDY,F-75010 PARIS,FRANCE

来源：

DIABETOLOGIA | 1994年 / 37卷 / 08期

关键词：

D O I：

10.1007/BF00404343

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

页码：842 / 842

页数：1

共 5 条

[1] A MUTATION IN THE TRANSFER RNALEU(UUR) GENE ASSOCIATED WITH THE MELAS SUBGROUP OF MITOCHONDRIAL ENCEPHALOMYOPATHIES [J].

GOTO, Y ;

NONAKA, I ;

HORAI, S .

NATURE, 1990, 348 (6302) :651-653

[2] 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

[3] DIABETES-MELLITUS ASSOCIATED WITH A PATHOGENIC POINT MUTATION IN MITOCHONDRIAL-DNA [J].

REARDON, W ;

ROSS, RJM ;

SWEENEY, MG ;

LUXON, LM ;

PEMBREY, ME ;

HARDING, AE ;

TREMBATH, RC .

LANCET, 1992, 340 (8832) :1376-1379

[4] MUTATION IN MITOCHONDRIAL TRANSFER RNA(LEU(UUR)) GENE IN A LARGE PEDIGREE WITH MATERNALLY TRANSMITTED TYPE-II DIABETES-MELLITUS AND DEAFNESS [J].

VANDENOUWELAND, JMW ;

LEMKES, HHPJ ;

RUITENBEEK, W ;

SANDKUIJL, LA ;

DEVIJLDER, MF ;

STRUYVENBERG, PAA ;

VANDEKAMP, JJP ;

MAASSEN, JA .

NATURE GENETICS, 1992, 1 (05) :368-371

[5] PREVALENCE OF MITOCHONDRIAL GENE-MUTATIONS IN FAMILIES WITH DIABETES-MELLITUS [J].

VIONNET, N ;

PASSA, P ;

FROGUEL, P .

LANCET, 1993, 342 (8884) :1429-1430

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