MYOTONIC-DYSTROPHY IS CLOSELY LINKED TO THE GENE FOR MUSCLE-TYPE CREATINE-KINASE (CKMM)

被引：46

作者：

BRUNNER, HG ^{[1
]}

KORNELUK, RG ^{[1
]}

COERWINKELDRIESSEN, M ^{[1
]}

MACKENZIE, A ^{[1
]}

SMEETS, H ^{[1
]}

LAMBERMON, HMM ^{[1
]}

VANOOST, BA ^{[1
]}

WIERINGA, B ^{[1
]}

ROPERS, HH ^{[1
]}

机构：

[1] CHILDRENS HOSP EASTERN ONTARIO,DIV GENET,OTTAWA K1H 8L1,ONTARIO,CANADA

来源：

关键词：

D O I：

10.1007/BF00283680

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：308 / 310

页数：3

共 27 条

[1] ALDRIDGE J, 1984, AM J HUM GENET, V36, P546
[2] A NEW PROBE FOR THE DIAGNOSIS OF MYOTONIC MUSCULAR-DYSTROPHY
BARTLETT, RJ
PERICAKVANCE, MA
YAMAOKA, L
GILBERT, J
HERBSTREITH, M
HUNG, WY
LEE, JE
MOHANDAS, T
BRUNS, G
LABERGE, C
THIBAULT, MC
ROSS, D
ROSES, AD
[J]. SCIENCE, 1987, 235 (4796) : 1648 - 1650
[3] Myotonia atrophica.
Batten, FE
Gibb, HP
[J]. BRAIN, 1909, 32 : 187 - 205
[4] Becker PE, 1977, MYOTONIA CONGENITA S
[5] NCOI RFLP AT THE CREATINE KINASE-MUSCLE TYPE GENE LOCUS (CKMM, CHROMOSOME-19)
COERWINKELDRIESSEN, M
SCHEPENS, J
VANZANDVOORT, P
VANOOST, B
MARIMAN, E
WIERINGA, B
[J]. NUCLEIC ACIDS RESEARCH, 1988, 16 (17) : 8743 - 8743
[6] EIBERG H, 1982, 6TH P INT C HUM GEN
[7] FEINBERG AP, 1984, ANAL BIOCHEM, V137, P266
[8] 3-POINT LINKAGE ANALYSIS EMPLOYING C-3 AND 19CEN MARKERS ASSIGNS THE MYOTONIC-DYSTROPHY GENE TO 19Q
FRIEDRICH, U
BRUNNER, H
SMEETS, D
LAMBERMON, E
ROPERS, HH
[J]. HUMAN GENETICS, 1987, 75 (03) : 291 - 293
[9] DIMORPHIC MARKERS FOR THE HUMAN APOLIPOPROTEIN-CII GENE LOCUS
FROSSARD, PM
COLEMAN, RT
FUNKE, H
ASSMANN, G
[J]. GENE, 1987, 51 (01) : 103 - 106
[10] NCOI RFLP AT THE HUMAN APOLIPOPROTEIN-CII GENE LOCUS
FROSSARD, PM
COLEMAN, RT
ASSMANN, G
[J]. NUCLEIC ACIDS RESEARCH, 1986, 14 (12) : 5120 - 5120